Abbott Laboratories (ABT) Q1 2022 Earnings Call Transcript

Abbott Laboratories (NYSE: ABT) Q1 2022 earnings call dated Apr. 20, 2022

Corporate Participants:

Scott Leinenweber — Vice President, Investor Relations

Robert B. Ford — Chairman and Chief Executive Officer

Robert E. Funck — Executive Vice President, Finance and Chief Financial Officer

Analysts:

Robbie Marcus — JPMorgan — Analyst

Vijay Kumar — Evercore ISI — Analyst

Joshua Jennings — Cowen and Company — Analyst

Larry Biegelsen — Wells Fargo — Analyst

Joanne Wuensch — Citibank — Analyst

Travis Steed — Bank of America — Analyst

Matt Miksic — Credit Suisse — Analyst

Presentation:

Operator

Good morning, and thank you for standing by. Welcome to Abbott’s First Quarter 2022 Earnings Conference Call. All participants will be able to listen-only until the question-and-answer portion of this call. [Operator Instructions] Should you become disconnected throughout this conference call, please redial the number provided to you in reference to Abbott earnings call. This call is being recorded by Abbott. With the exception of any participant’s questions asked during the question-and-answer session, the entire call, including the question-and-answer session is material copyrighted by Abbott, it cannot be recorded or rebroadcast without Abbott’s expressed written permission.

I would now like to introduce Mr. Scott Leinenweber, Vice President, Investor Relations, Licensing and Acquisitions.

Scott Leinenweber — Vice President, Investor Relations

Good morning, and thank you for joining us. With me today are Robert Ford, Chairman and Chief Executive Officer; and Bob Funck, Executive Vice President, Finance and Chief Financial Officer. Robert and Bob will provide opening remarks. Following their comments, we will take your questions. Before we get started, some statements made today may be forward-looking for purposes of the Private Securities Litigation Reform Act of 1995, including the expected financial results for 2022. Abbott cautions that these forward-looking statements are subject to risks and uncertainties that may cause actual results to differ materially from those indicated in the forward-looking statements. Economic, competitive, governmental, technological, and other factors that may affect Abbott’s operations are discussed in Item 1A Risk Factors to our Annual Report on Form 10-K for the year ended December 31, 2021.

Abbott undertakes no obligation to release publicly any revisions to forward-looking statements as a result of subsequent events or developments except as required by law. On today’s conference call, as in the past, non-GAAP financial measures will be used to help investors understand Abbott’s ongoing business performance. These non-GAAP financial measures are reconciled with the comparable GAAP financial measures in our earnings news release and regulatory filings from today, which are available on our website at abbott.com.

Note that Abbott has not provided the GAAP financial measure for organic sales growth on a forward-looking basis because the Company is unable to predict future changes in foreign exchange rates, which could impact reported sales growth. Unless otherwise noted, our commentary on sales growth refers to organic sales growth, which excludes the impact of foreign exchange.

With that, I will now turn the call over to Robert.

Robert B. Ford — Chairman and Chief Executive Officer

Thanks, Scott. Good morning, everyone, and thank you for joining us. Today, we reported results of another strong quarter. Earnings per share were $1.73, reflecting more than 30% growth compared to the prior year. Sales increased 17.5% on an organic basis in the quarter, led by double-digit growth in Medical Devices, Established Pharmaceuticals, as well as Diagnostics, both with and without COVID testing-related sales. In addition to the strong results during the quarter, we continue to strengthen our strategic position and long-term growth opportunities with regulatory approvals of new products and expanded indications of use along with continued market uptake of several recently launched products in attractive growth areas.

I’ll now summarize our first quarter results in more detail before turning the call over to Bob. And I’ll start with Established Pharmaceuticals or EPD, where sales increased 13.5% in the quarter. EPD has now achieved double-digit organic sales growth in three of the last four quarters. Strong performance this quarter was led by double-digit growth across several countries and core therapeutic areas, including gastroenterology, respiratory and CNS pain management.

Turning to Nutrition, where our performance was mixed. Our Adult Nutrition business continues to perform at a high level with global organic sales growth of 11.5%, led by our Ensure and Glucerna brands. And we also achieved double-digit growth globally in our combined toddler nutrition products, which includes our market leading PediaSure and Pedialyte brands. As you know however, we initiated a voluntary recall in February of certain infant formula products manufactured at one of our U.S. facilities. It’s important to highlight as part of our quality system, we retain in-house samples of products that we ship to customers.

Testing of retained samples related to this recall action by both Abbott and the FDA have all come back negative for the presence of the bacteria that cause the reported illnesses. Importantly, the FDA and CDC found that there is no genetic match between the strains of the bacteria identified in non-product contact areas of our facility and available samples obtained from customer complaints, suggesting a different source of contamination. And lastly, no Salmonella was found in our factory or product, and therefore, the FDA ruled out any link to our facility.

We hope these findings give [Phonetic] parents, caregivers, and other stakeholders renewed confidence in our products. We know the situation has further exacerbated industry-wide infant formula supply shortages. That’s why we’re doing everything possible to mitigate supply constraints by bringing in product from our FDA-registered facility in Europe and ramping up production at our other U.S. plants. And, of course, we’re working very closely with the FDA on corrective actions and enhancements, so that we can restart operations at the facility.

Moving to Diagnostics, where sales grew 35%. COVID test sales were $3.3 billion in the quarter, more than 90% of which came from our rapid tests, including BinaxNOW in the U.S., Panbio internationally, and ID NOW globally. Excluding COVID-related test — COVID testing-related sales, our global diagnostic sales grew 12% in the quarter, driven by the continued roll-out of Alinity, our innovative suite of diagnostic instruments and expanding menus across our testing platforms.

And I’ll wrap up with Medical Devices, where sales grew 11.5% in the quarter. This strong performance was led by double-digit growth in Diabetes Care, Structural Heart, Heart Failure, and Electrophysiology. In Diabetes Care, sales of FreeStyle Libre grew more than 25% on an organic basis in the quarter and the user base has now reached approximately 4 million users globally. In Cardiovascular Devices, while procedure volumes were negatively impacted by elevated COVID case rates early in the year, we saw steady improvement in procedure trends as the case rates came down in the second half of the quarter, which has continued into April. In addition to improving market trends and our strong results, this was also another highly productive quarter for our pipeline.

In the U.S., we received FDA approval for Aveir, our leadless pacemaker to treat patients with slow heart rhythms. In Japan, expanded reimbursement for Libre will now cover all people with diabetes who use insulin at least once a day. CardioMEMS received an expanded indication in the U.S. to treat more patients suffering from earlier stages of heart failure. And we received U.S. FDA clearance for the latest generation of our EnSite X System, which provides a 360 degree view of the heart for improved cardiac mapping.

So in summary, we’re achieving strong growth overall and across several areas of our business. As the first quarter progress and COVID levels decrease, we saw a steady improvement in the hospital-based procedure trends, which has continued into April. And we continue to advance our pipeline with new products, indications, and reimbursement coverage in several attractive growth areas.

I’ll now turn over the call to Bob. Bob?

Robert E. Funck — Executive Vice President, Finance and Chief Financial Officer

Thanks, Robert. As Scott mentioned earlier, please note that all references to sales growth rates, unless otherwise noted, are on an organic basis, which excludes the impact of foreign exchange.

Turning to our results. Sales for the first quarter increased 17.5% on an organic basis, which was led by double-digit growth in Diagnostics, Medical Devices, and Established Pharmaceuticals, along with global COVID testing related sales of $3.3 billion in the quarter. Excluding COVID testing related sales, organic sales growth was 7.7% versus the prior year. Foreign exchange had an unfavorable year-over-year impact of 3.7% on first quarter sales. During the quarter, we saw the U.S. dollar continue to strengthen versus several currencies, which resulted in a more unfavorable impact on sales compared to exchange rates at the time of our earnings call in January.

Regarding other aspects of the P&L, the adjusted gross margin ratio was 59.1% of sales, which reflects higher than normal fall-through on COVID testing sales as a result of significant production volumes during the first quarter, partially offset by the impacts of the Nutrition recall and somewhat higher than expected inflation on certain manufacturing and distribution costs in the quarter. Adjusted research and development investment was 5.6% of sales and adjusted SG&A investment was 23.1% of sales in the first quarter. Lastly, our first quarter adjusted tax rate was 14.5%.

Before discussing our outlook for the full-year, I want to provide an update on our strategic capital deployment initiatives completed in the first quarter, which included approximately $2.3 billion of share repurchases, $800 million of dividends, scheduled debt repayment of $750 million, and $300 million of capital expenditures, which support future organic growth opportunities. We continue to generate strong cash flow, which provides the flexibility required to execute a well-balanced capital allocation strategy.

Turning to our outlook for the full-year 2022. Our adjusted earnings per share guidance of at least $4.70 remains unchanged. We now forecast total Company organic sales growth, excluding the impact of COVID testing-related sales to be in the mid to high single-digits, which is somewhat lower than our prior forecast of high single-digits due to the recent recall event in Nutrition. It is important to note, excluding sales impacted by the recall, we continue to forecast total organic sales growth in the high single-digits for the remainder of our combined businesses, which includes Medical Devices, Established Pharmaceuticals, Diagnostics, excluding the impact of testing-related sales and areas of Nutrition not impacted by the recall.

We forecast COVID testing-related sales of approximately $4.5 billion with a significant portion of these sales expected to occur in the first half of the year. We continue to — we’ll continue to update our COVID testing-related sales forecast one quarter at a time throughout the year as appropriate. Lastly, based on current rates, we would now expect exchange to have an unfavorable impact of a little more than 3% on our full-year reported sales.

With that, we’ll now open the call for questions.

Questions and Answers:

Operator

Thank you. [Operator Instructions] And our first question comes from Robbie Marcus from JPMorgan. Your line is open.

Robbie Marcus — JPMorgan — Analyst

Hi, good morning. Thanks for taking the question, and congrats on a good quarter. Maybe to start for Robert or Bob, you guys put up a good first quarter being on COVID testing sales had double-digit growth in most of the businesses. I was hoping maybe you can reconcile the strong 1Q and the reiterated guidance and walk us through some of the puts and takes and how to think about bridging the difference?

Robert B. Ford — Chairman and Chief Executive Officer

Sure, Robbie. I think you’ve been on these calls for a while. We rarely raised in Q1, I would say. And despite that, I mean, we’ve had a great start to the year as you pointed out, and there’s a lot of good things going on at the Company. We talked a little bit about procedure recovery in the comments. We’ve seen good recovery in our device portfolio, especially in cardiovascular, seen routine diagnostic testing improving albeit a little bit slower than what we’ve seen in devices, but definitely the trend of recovery is there, EPD execution is going very well, like I said in the comments, three out of four quarters, double-digit, strong COVID sales, both in the U.S. and internationally. And I think that’s an important aspect here is our international presence too.

Talked a little bit about the pipeline and the approvals, not just the recent approvals, but the performance of some of the recently launched products. Bob talked about our cash flow generation and the deployment of that cash flow. We’re able to kind of share part of that cash flow with our shareholders, but also to continue to invest in the business. So there’s a lot of good things going on here in the business, and — but there are — there’s — there are a couple of challenges that we’re managing, and that’s probably the piece there where the reconciliation that you’re looking for is actually happening.

First of all, obviously managing through the recall on the Nutrition side, we’re working with the FDA. And we’ve contemplated in that reiterated guidance, various scenarios here in terms of kind of restart dates and share recovery curves, etc. So it’s difficult to give an exact date right now as to when that restart starts. We’re working closely with the FDA, but I see this more as a shorter-term challenge in the sense that once we align with restarting with the FDA then we’ll begin to execute our strategy here in terms of coming back to market, resupplying the market and regaining the share.

Probably the second other part here, which is I think is a little bit not unique to Abbott. And I think you’ll probably see this across a lot of companies is just the macroenvironment right now has definitely changed versus where we were in January, and it’s gotten a little bit more challenging. So — and I — we expect some of that macroenvironment, whether it’s supply chain, etc., to kind of be a little bit more persistent throughout this year. So that being said, wanted to see how these — probably these two points here play out over the next couple of months, and we’ll be in a better position to be able to assess that and on our guidance going forward after Q2.

But like I said, there’s a lot of great momentum in the business, devices performing very well, Diagnostics performing very well, the parts of Nutrition that weren’t impacted by the recall continue to do very well. I’m not a big fan of the, exclude this, but for that statements, but I think in the context of how the business is performing, I mean, if you exclude the COVID piece, which was pretty significant for us and then just look at the business without the base business, without the impacted Nutrition products, our growth rate was about 11%. And I think that reflects the strength of the portfolio, the investments that we’ve made and the execution. So in that guidance, that reiteration of $4.70, we’ve absorbed, as Bob said, more FX headwinds, absorbed some challenges in supply chain, absorbed portions of the Nutrition recall. So I think it’s the right EPS guide right now in terms of where we are after Q1.

Robbie Marcus — JPMorgan — Analyst

Great. Really good color. And maybe as a follow-up, I think a lot of investors are focused on the go-forward, realizing that January and February weren’t the strongest months due to some of the elevated Omicron levels. So we heard Johnson & Johnson yesterday talk about reaching pre-COVID volume levels in April. It sounds like you exited and continue to see strong growth coming out of the quarter and into second quarter. I was hoping maybe you could give us a little more color on just the volume trends you’re seeing particularly in devices and diabetes, which was one that missed the street a little bit in the quarter? And how you’re seeing the geographic spread and any differences there? Thanks a lot.

Robert B. Ford — Chairman and Chief Executive Officer

Sure. I mean I think the story-line here was very similar, as I said in my comments. I mean it started off a little bit slower than we had anticipated in January, obviously, given Omicron and the surges there and the pressure that, that put on staff at hospitals. But definitely sequential improvement from a dollar perspective every month as we moved along the quarter, March was very strong. I’ve always talked about how we compare our businesses versus pre-pandemic levels to kind of avoid some of the comp issues that ultimately do exist.

If you look at our Q1 ’22 growth rate versus 2019, we were up about 7.3%. So well ahead of where we were in 2019. And that was pretty broad-based. Geographically, the U.S. was up 6%, again versus 2019, and international was up over 8% versus 2019 too. So I think our Device business has performed very well, and we’ve seen that improvement as we went through the quarter. The cardiovascular side has done very well as I’ve kind of given those numbers, and March was really strong too.

I think it’s part of it is recovery, Robbie, that we’re seeing. But also — I would also put in those numbers, I made these comments about recently launched products that we started launching last year. It’s always a challenge to launch these new technologies in that COVID environment, but it was the right decision to make, and we’re seeing good momentum on whether it’s Amulet, Navitor in Europe, CardioMEMS, the roll-out of EnSite X that began in Q4 of last year, our TriClip product. So I think all of that, it’s the combination, I would say of both recovery as the COVID cases subside, but also the new product launches in the pipeline that we put, which is driving this performance where I’d say we’re ahead of where we were in 2019 having good growth rate in our cardio portfolio.

Robbie Marcus — JPMorgan — Analyst

Appreciate the color. Thanks.

Operator

Thank you. Our next question comes from Vijay Kumar from Evercore ISI. Your line is open.

Vijay Kumar — Evercore ISI — Analyst

Hey guys, thanks for taking my question. Robert, maybe back on this guidance question, right, the testing guidance was raised by $2 billion [Phonetic], right, that’s perhaps $0.40 of upside, and reiteration of this EPS, like what is offsetting this — the incremental tailwinds from COVID rates, like how much of this is FX, was this macro Russia versus the recall or inflationary pressures, I think a little bit more granularity will be helpful?

Robert B. Ford — Chairman and Chief Executive Officer

Sure. Well, I mean I think you hit on the key points there. I mean inflation — additional inflation pressures is impacting some of that. We’ve got a couple of $100 million that we’ve contemplated throughout the rest of the year in terms of friction on supply chain costs, input costs, freight and distribution. The recall, well, let me take a step back, the FX is probably about another about $0.05 of friction that we’re having as we’ve seen the dollar strengthen, and the rest of it is really coming from Nutrition, but it’s very difficult right now, Vijay, to be able to kind of pinpoint exactly. We’ve got a couple of different scenarios as I said in the first question in terms of the restart and the curve. So we are seeing more COVID tests and more COVID sales, and that, like I said, is absorbing some of these challenges.

Vijay Kumar — Evercore ISI — Analyst

Understood. And then one on Libre. Sequentially, revenues declined, and I guess my question is, you’ve been adding, I think a couple of 100,000 new patient starts. Is that new patient starts changing at all? How should we think about the incremental reimbursement in Japan? And was this seasonality or what drove the sequential Libre revenue trends?

Robert B. Ford — Chairman and Chief Executive Officer

Yeah. I mean I think we see some of that from time to time here, especially as you go from Q4 to Q1, Vijay. We’ve seen that a couple of times. I’d say internationally, the biggest driver of that is actually FX that created that. We’ve seen good growth internationally from Libre getting close to 20% on a very large base. And in the U.S., you’re going to see some timing patterns there in terms of wholesaler ordering. I like to look at scripts, both new-to-brand scripts and total Rx scripts here in the U.S., and the sequential Q1 to Q4, there’s definitely growth there.

So I think we’ve done a really good job in the U.S. We’ve grown our business in this quarter by 50%. Users now well over 1 million users. We’ve made the investments in the U.S., whether it’s salesforce, DTC advertising, I think the team is beginning to hit its stride over there. They know that I’m not satisfied. We always want to see more and believe that we can do more. But I think the U.S. is starting to kind of really hit its stride with those investments as the salesforce gets deployed and establishes the relationships with what is new physicians that are getting introduced to CGM. So I think that’s worked out very well. If I take a step back though and move away a little bit from the Rxs and the sequential, I think one of the key things here to really take a look at is the evolution of the CGM market.

And I’m starting to really see now what we had always envisioned this market to start to be, which is a market that is shifting from what traditionally was more of a Type 1, more of a pumper — insulin pump kind of connectivity play, which is an important segment, but really start to move and expand beyond that. And we’re starting to see signs of that, and I think Libre is a big driver. The value proposition of Libre is a big driver, whether it’s physicians and payers quite frankly starting to see the value of the sensing technology across the — across a much broader set of patients. If you look at a U.S. base of patients, and we get to see this because we get to see the Rx data in terms of what medications the patients are using.

And over 40% of our user base, which is pretty large in the U.S. is already Type 2 non-intensive. And that, as I said, is really kind of the opportunity to expand this market and become a really strong growth driver. The Japan reimbursement that you just referenced, again, this goes back to a comment I made about, we see this as a mass market opportunity. So counter to maybe how we think about reimbursement in different segments of devices where you’re thinking about price of reimbursement versus patient TAM, we’re looking at patient TAM much more than we are on the pricing side.

We’ve got great reimbursement in Japan, but to be able to have access to all of — all insulin users in Japan with our product is a great opportunity for us. And then you’re seeing the value proposition, again, really strong. There was a study that was published by U.K. NICE. And I think that for me is the ultimate validation of our strategy and the value proposition we offer, where it was clearly shown to be extremely cost effective, whether you look at ICERs or QALYs in the U.K. by NICE and their view here of how this can benefit a lot of patients. So that for me is the real exciting part of Libre is we’re really starting to see that evolution from the CGM market to become much more than kind of a niche play and much more a mass market play. And I think we’re starting to see evidence of that, whether it’s new studies or reimbursement access or even seeing physicians, primary care docs start to really embrace the prescription of CGM for Type 2s. So…

Vijay Kumar — Evercore ISI — Analyst

That’s helpful, Robert. Thank you.

Operator

Thank you. Our next question comes from Josh Jennings from Cowen. Your line is open.

Joshua Jennings — Cowen and Company — Analyst

Hi, good morning. Thanks for taking the questions, and congratulations on a strong start to the year. Rob and Bob, I just wanted to start with just a question on gross margins. The 1Q performance was the highest since 20 — quarters in 2019. Just wanted to better understand the sustainability of this profile, that 59.1% [Phonetic] despite all the challenges in place in 1Q? And then — and should investors be thinking that return to 2019 gross margin levels in that 59% range plus is achievable in the out-years? And then the follow-up is on MitraClip.

I just wanted to hear — and Amulet is, what have you learned in the early days, the Amulet launch as the number two player in the U.S. left atrial appendage closure market that you can apply to your defense strategy starting this year, maybe carrying into next year when you’re defending your MitraClip turf as the number one player assuming the U.S. Pascal launch occurs in 2023? Thanks for taking the questions.

Robert E. Funck — Executive Vice President, Finance and Chief Financial Officer

Okay. Josh, I’ll take the kind of the gross margin question. In the first quarter, our gross margin certainly benefited from the very high COVID testing sales. As I mentioned in my remarks that actually the fall-through on that was higher than we’ve seen in the past because of the production volumes that we had going through our plant, we’re basically running full out on that. So our first quarter definitely benefited from that. As we look at the rest of the year, obviously, we’re going to have to have the impact of the Nutrition recall and the inflation, the increased inflation that Robert mentioned, obviously, inflation is not unique to us.

As we said back in January, we incorporated a sizable amount in our guidance at that point in time. And what we’ve seen and I think a lot of other companies have seen is kind of an increase in some of those headwinds. And so we’ve captured that in our guidance for the rest of the year. When I think out beyond this year and where gross margin goes, I mean, gross margin is something we focus on in the Company constantly. We’ve got dedicated teams within each business that are focused on driving gross margin improvements. I mean, a lot is going to depend, I think as we think out in the future, the evolution of inflation and supply chain dynamics and how those evolve over time, that will be a key component. And then obviously, as we grow the top-line in our Medical Device business, that’s accretive to the overall profile of the Company. And so that’s kind of where we see gross margin right now and potentially in the future.

Robert B. Ford — Chairman and Chief Executive Officer

Yeah. On your question on MitraClip and Amulet, so I’ll talk a little bit about MitraClip. I’d say the progression of MitraClip in the quarter was very similar to my commentary on our cardiovascular procedure, right? So we obviously had high COVID case kind of impact that — but started to really accelerate growth towards the end of February and into March. So as those cases came down, we saw the improving growth rate. But I’ll tell you, I mean, while the growth rate has been strong and it’s been strong for while, Josh, I don’t think we’ve really been able to benefit yet from the FMR indication, which we got kind of right in the middle of COVID.

And as part of that, and I talked a little bit about this, to be able to benefit from this pretty significant kind of market expansion opportunity that we had with incredible robust data from COAPT, you have to really start to work those patient referrals and the referral networks. And we began doing that when COVID took its first break and then that got put on hold again when Delta and Omicron served. So I’m really looking forward and the team is kind of already putting in place that strategy again to reengage the patient referral network, so that we can really take advantage of this indication, which is unique to us and will be unique to us for a while. Relating to competitive movements onto the market, we just got to stay ahead.

We’ve got to keep on investing in the product. So we’ve done that with MitraClip, staying ahead and iterating and improving on the performance of the product. We’re investing in new trials. I talked about our investment that we’re making in moderate risk surgery patients, that will be a great opportunity for us. And we have a great team, and we have great relationships and a strong mitral position. So not discounting the fact that we’ll have competition. We’ve had competition in Europe for a couple of years already. Germany is probably the second largest global market, and our position there remains at an 80% market share.

So acknowledge that we will have competition, but we do — we have established this mitral leadership position, and we intend to defend it because of all the investments that we’ve made to create this market. So that’s what I would talk about MitraClip. I still think the best is still to come because I don’t think we’ve been able to tap into the opportunity of the FMR indication. Regarding Amulet, listen, I think the team has done a really good job, again, reiterating the same kind of comments, a little bit challenged in the beginning of the quarter. And that was predominantly driven by the fact that we wanted to start the initial cases with every case being proctored.

So difficult to move proctors throughout the U.S. and travel international, etc. So that slowed us down a little bit in the beginning of the year. But I’ll tell you, the team has done — we spent a lot of time and attention and focus with them in February and March. And the team has definitely had a really strong exit to Q1, caught up in terms of all the contract closes that we had established as part of our plan in Q1. So I think the commercial execution is doing really well, and that’s supported really by the performance of the product.

And once physicians have had an opportunity to get a couple of these implants done, it’s a little bit of a different technique, but they feel comfortable with it and then they get the benefits of what the data shows is superior closure, and that’s really because of our unique dual sealing mechanism. So there was some data that came out — late-breaking data that came out of the ACC, which talked about the importance of leaks and leaks matter, whether they’re big leaks or whether they’re small leaks, they do matter. And even the small leaks were associated with an increase in thromboembolic events. So I think we’re in a good position now with Amulet. I’m pleased with the commercial team and what they’re doing in the clinical team, and we’ve got opportunities here to grow. I think momentum is building with Amulet.

Joshua Jennings — Cowen and Company — Analyst

Thanks so much for all that color. Appreciate it.

Robert B. Ford — Chairman and Chief Executive Officer

Yeah.

Operator

Thank you. Our next question comes from Larry Biegelsen from Wells Fargo. Your line is open.

Larry Biegelsen — Wells Fargo — Analyst

Good morning. Thanks for taking the question. So Robert, two high-level questions for me. One, I’ll push my luck a little bit and see if we can get any preliminary thoughts on 2023. You’re getting a meaningful testing benefit this year, which may not materialize next year. So how do you feel about your ability to grow margins and earnings next year as testing demand drops? And I had one follow-up.

Robert B. Ford — Chairman and Chief Executive Officer

Sure. Well, we had a really strong quarter regarding testing, Larry. And I think to answer your question, I think you have to kind of look at what’s going on a little bit right now in the U.S. and internationally. In the U.S., we saw cases decline pretty significantly in February. But I think we all agree that some of those cases that are being reported aren’t covering all cases because of the use of the at-home testing systems, right, that are currently available. So I think that’s part of the process that we’re seeing as testing as we’re moving more into this kind of endemic state. And as we move to this endemic state, listen, vaccines have been incredibly powerful to be able to prevent serious illness to be able to protect the hospitals and the hospital system, but it’s really testing that really allows us to kind of move to this endemic state and kind of live our day-to-day and it’s more about surveillance and screening and checking.

So — and I think our product has done really well here. It’s maintained a kind of preferred status here in the U.S., even with a pretty significant increase in product coming into the country, whether it’s ease of use, its shelf life, the reliability it has, its studies, etc. So I think that, that’s an important aspect as we go into 2023 is, do we have confidence that even in an endemic state does testing continue? And I would say, yeah, it does continue. One portion that doesn’t get a lot of attention is our international testing business.

50% of our sales in March of COVID tests came from the international markets. And I’d say, similar sense there of governments investing in testing and coming to Abbott as one of the preferred suppliers. So I think that to answer your question, obviously, there’s a certain amount that you can’t overcome, right? But I do think that as we go into next year, we’ll have a portion of our testing business that will look more like a flu kind of respiratory kind of endemic state, and I think that’s going to be important as we continue to grow earnings.

And then on top of that, like I said, the focus of our Medical Device business, the investments we’ve made in our diagnostic systems and increasing the test menus over there, so I expect our base business to continue to grow very strongly. Yeah, it’s a little bit early regarding 2023, but we are planning. We are looking. We are looking at where we’re going to be able to kind of grow, and I’d say there will be some COVID business next year. I think we’re in probably the strongest position to be able to kind of capitalize and lead in that market. And then our base business is going to do very strongly next year with all the investments we’ve made and new product pipeline that we’ve got.

Larry Biegelsen — Wells Fargo — Analyst

That’s super helpful. And Robert, you’re in a unique position with your strong balance sheet. I saw you mentioned on the call, you bought back, I think $2.5 billion in stock this quarter. What’s your — what are your updated thoughts on M&A? And if you can’t find attractive assets, are you going to continue to return cash to shareholders like we saw this past quarter? Thank you.

Robert B. Ford — Chairman and Chief Executive Officer

Sure. On the M&A side, yeah, I mean, I’ll sound like a broken record here, Larry. I mean we’re always looking. We’re always studying. We’re always looking at ways to be able to add to the Company and add to our business, but it needs to be strategic. And from that perspective, I don’t want to dilute our growth rate, I don’t want to dilute our profiles. We need to make sure that we’re looking at assets that will be additive to our growth rate into our profile. So at least the top-line. So that’s always there and we’re always looking. Regarding the approach, listen, it’s always a balanced approach, Larry. We’re generating strong cash flow. We got a lot of financial flexibility here. We’ll return $3 billion when you — in terms of dividend this year. Bob talked about what we’ve done regarding buybacks. And we’re always going to look at this kind of balanced approach.

We’ve made investments in our organic opportunities for growth because I believe that those are great returns for our shareholders, whether it’s Libre, MitraClip, expansion of our Medical Devices, Diagnostics, those are all opportunities that deliver great returns for our shareholders, and we’ll take that balanced approach. And if there is an opportunity for more, we’ll do more.

Larry Biegelsen — Wells Fargo — Analyst

Thanks so much, Robert.

Robert B. Ford — Chairman and Chief Executive Officer

Yeah.

Operator

Thank you. Our next question comes from Joanne Wuensch from Citibank. Your line is open.

Joanne Wuensch — Citibank — Analyst

Good morning, and thank you very much for taking the question. I’d like to circle back a little bit to the nutritional business. A lot of the feedback that I get from investors is some level of concern regarding brand name, brand damage, if you will. And I’m curious your thoughts on what it would take to sort of revamp this business up?

Robert B. Ford — Chairman and Chief Executive Officer

Sorry, you’re referring to Nutrition business?

Joanne Wuensch — Citibank — Analyst

Yes.

Robert B. Ford — Chairman and Chief Executive Officer

Okay. Listen, we’ve got a very robust manufacturing network and a robust quality system. Obviously, there’s a shortage of product in the market. I highlighted some of the things that we’re doing to be able to kind of resupply the market. A key aspect of that is going to be the restart, and we’re in that process. We’ve got a strong brand with Similac. We — we’ve maintained a lot of contracts. We’ve been able to supply those contracts even with a little bit of this shortage.

So I feel confident in our team’s ability here to look at once we get restarted to be able to resupply the market and build back our share. We had just launched a new product last year, end of last year with a blend of 5 HMOs, and that’s a significant advancement. And we were expecting that based on everything that we had studied and seen was going to be a big growth driver for us and kind of brand enhancers. So I think that’s going to be important. And yeah, we’ll have to make some investments as we go back to the market. But I’d say historically, when some of these issues have happened in the past, whether it’s Abbott or other manufacturers, share does recover. The question is just kind of the timing and the curve of that recovery, but share do come to recover and you can look at past situations with other competitors and even with us.

Joanne Wuensch — Citibank — Analyst

Thank you. And as a follow-up, forgive me for asking it this way. What’s next? I mean, I don’t think we’re going to be talking about COVID testing in a year. I hope we’re not going to be talking about it. But how do you see the sort of forward momentum of the Company, big picture? Thanks.

Robert B. Ford — Chairman and Chief Executive Officer

Yeah. Well, yeah, I don’t think we’re going to be talking about COVID testing the way we’re talking about it today or how we talked about it in the past year. But like I told Larry, I mean, I do think that there’s going to be an opportunity for COVID testing to play a role in this kind of endemic state. And as I’ve said in the past also, what COVID has allowed us to do is to further accelerate what we believed was a key trend in diagnostics and point-of-care diagnostics, which is the expansion and the decentralization of that testing outside of the lab into pharmacies, into people’s homes and it being connected.

So I think that — COVID has accelerated that, I guess, I would say. And we’re obviously building menus, where we’ll be able to add to the ID NOW instrument, more panels, more different tests. Remember, when we started the pandemic, we had about 20,000 kind of instruments, that’s now five-fold in terms of the opportunity that we have to be able to expand menu into basically an asset that’s been capitalized and deployed into the market. So that’s what we’ve been working on from that perspective on the, I guess, I would say, on the rapid testing side, on the decentralized testing side. I’d say going back to the device portfolio, I mean there’s still a lot of what next in our pipeline of products that we’ve just launched that are still in the early — still in the early innings here. One of them that we got approved this quarter, which I’m really excited about, is Aveir and our leadless pacemaker. I think this is going to be a great opportunity to kind of reignite growth back in our CRM business.

I mean we’ve seen an improvement already with the existing portfolio and had a 4% growth this quarter. But I think Aveir is a real kind of game changer for our CRM portfolio. Obviously, the single-chamber is a smaller part of the market. We know that it’s about 15%. But I think when you’re coming second to the market, you get to observe what needs to — what could be addressed that maybe the first generation didn’t do. And I think that our product, whether it’s retrievability, its ability to be retrieved, it’s longer-lasting battery, right now, it’s about 2x product that’s on the market. But I think what’s really exciting about this is its ability to upgrade to a dual-chamber device.

So it’s upgradability is what we’re hearing extremely big interest from the physician community. So I think that’s a great opportunity for us that I think is really going to start to show as we evolve our trial for dual-chamber and begin to collect data there, I think that’s going to be a great opportunity for our CRM portfolio. I look at CardioMEMS as another great opportunity that we have just really just started. The expanded indication is going to really open up the market. I’ve seen some of the implant trends that we’ve seen post-expansion indication, and that gives me a lot of excitement about what this product can be.

We talked about Amulet. I think that the TAVR piece is one that, where — as I’ve said in the past, where we’re investing. I think Navitor is an extremely competitive product, and we’re seeing that in Europe as we’ve launched it and been six months in the market now. So there’s great opportunities over there. Libre 3 is an opportunity for us, not only in the U.S., but in Europe to continue to expand the market. I think Lingo, as I said last call, is another great opportunity that is really in the early stages, but to look at using our biowearable sensors outside of diabetes and looking at opportunities there. So I think we have a lot of what next that are truly early in the — in their early stages. And then on top of all the products that we’ve been talking about right now also. So I’m excited about the what next.

Joanne Wuensch — Citibank — Analyst

Thank you.

Operator

Thank you. Our next question comes from Travis Steed from Bank of America. Your line is open.

Travis Steed — Bank of America — Analyst

Hi, good morning. Thanks for taking the questions. First, on the inflation supply chain, sound like it’s gotten about $200 million worse than $500 million you had built into the P&L, just to confirm that? I’m curious what you’re seeing the biggest pain points? Is it wages, raw materials, shipping costs and expectations on when that could start to ease to some degree or how you’re thinking for a potential offset to [Phonetic] price?

Robert E. Funck — Executive Vice President, Finance and Chief Financial Officer

Yeah. Travis, I’ll take the question. This is Bob. So as we said back in January, we did incorporate a sizable impact into our 2022 guidance, which was about $500 million on the gross margin line. And as Robert mentioned, we’ve now incorporated an additional $200 million in gross margin impact in our current guidance. The biggest impact we’re seeing is really on logistics and commodities and some other manufacturing inputs. It’s not so much on the labor front.

Labor is a smaller portion of our total product cost. So it’s really on the commodities. In terms of when this will ease and change, I mean, that’s a very — I think there’s a lot of things that affect that and where the — where inflation may go. We do know that historically on commodities, we do see cycles. We do see commodity costs go up, but they also come down. And we would expect at some point, and it’s very difficult to kind of call exactly when that will be, we will see some of the inflationary pressures subside.

Travis Steed — Bank of America — Analyst

And then given your presence in China, I’d just kind of love to hear your thoughts on both China from a procedure standpoint and also a supply chain standpoint, just given how much of a business you have there? And any thoughts on the progress you’re making with Libre 3 and the FDA would be great too? Thank you.

Robert B. Ford — Chairman and Chief Executive Officer

Sure. I think regarding China, saw a little bit of an inverse in terms of what we saw in all the other geographies where started off pretty well in the quarter, and then as the lockdown started to occur, specifically in Shanghai towards the end of February and into March, started to kind of see the impact of that in our procedures. We look at our testing platforms as kind of a early indicator and a proxy. So we saw those go down also during the month of April — during the month of March. And I’d say, over the last two weeks in April, started to see a recovery of those diagnostic testing.

So I think what we saw was a lot of the testing that was being done in the major kind of cities was shifted over to kind of PCR testing together with rapid testing and that obviously impacted some of the routine hospital testing. But we’re starting to see that now probably two solid weeks of kind of positive trend back in the right direction, still not at the level we were before the lockdowns, but definitely starting to move in the right direction there. So I would expect just based on patterns that we’ve seen in the past that we’re starting to kind of move to sequential week-over-week improvements in the procedures. And not all procedures are the same, some of them return faster, some of them have a different kind of recovery curve. But I do expect kind of the impact that we saw in March and a little bit in the beginning of April on devices start to kind of improve. Sorry, you had a question on Libre 3?

Travis Steed — Bank of America — Analyst

Yeah, Libre 3. Any update on how the progress is working with the FDA or what the label might look like, just any additional color would be great? Thank you.

Robert B. Ford — Chairman and Chief Executive Officer

Sure. Like I mentioned in the call, we filed as an iCGM. I don’t have much to kind of update you there regarding that. I will say that it — we have moved Libre 3 in Europe into — from kind of more of a limited roll-out in Germany a while back to kind of more of a accelerated conversion from Libre 2 to Libre 3. And I think the process started really well in Germany. We got initial feedback from physicians, very positive feedback from the reimbursement system also. And that gave us the confidence here to kind of really begin to accelerate this market transition in Libre 3.

We did that in Libre 2 also when we moved from Libre 1 to Libre 2 in Germany. That took us about a year. I think it’s going to be faster than that with Libre 3. And we’ve got over 90% reimbursement coverage for Libre 3 in Germany. So that’s now moved into high gear, not only in Germany, but for the rest of the year. So I’m focused a lot on what we can do with Libre in the countries that we do have it approved. And right now, everything that we’re seeing is that it is a very, very compelling product.

Travis Steed — Bank of America — Analyst

Great. Thanks a lot.

Scott Leinenweber — Vice President, Investor Relations

Okay. Operator, we’ll take one more question.

Operator

Thank you. Our last question will come from Matt Miksic from Credit Suisse. Your line is open.

Matt Miksic — Credit Suisse — Analyst

Hey, thanks so much for squeezing me in. Just in the context of some of these new products, I did want to maybe follow up with just a level set expectations, for example, the Alinity roll-out and menu expansion, very strong growth in the quarter. Robert, if you could maybe talk about what’s the duration of this roll-out? I know it started into the pandemic. And what does that look like through this year and potentially through next year? And then I know you touched this a few times here about Amulet. Just love to get your updated thoughts on where you think share could go in the next year, 18 months? You’ve made some comments in Q4. I know the pace is picking up here in the U.S. Any numbers you could put around your thoughts there would be super helpful?

Robert B. Ford — Chairman and Chief Executive Officer

Sure. I mean Alinity is a multi-year strategy and roll-out here, Matt. We’re doing it not only with immunoassay, we’re doing with clinical chemistry, we’re doing with hematology, we’re doing it with transfusion. This has never been done at this kind of scale to be able to really recycle all of our systems. So I think that if you look at the way the market is set up, the contracts are lasting between 7 to 10 years. So on any given year, you’ve got 15% of the market that’s coming up for an RFP.

So regarding its legs like you’re asking, I mean, I still think that we’ve got multiple, multiple years here. The COVID pandemic definitely slowed that down in terms of the renewal cycles, a lot of hospitals focusing on just dealing with the COVID. But I guess what I would say is there’s plenty more to come. The key here is the balance between — in that 15% that comes up for RFP, what’s renewable to an existing customer and what’s kind of share gain. And I think the team has done a really good job at being able to look at having a real strong balance about not just defending the base, and we’ve done that pretty well. So I’d say, 9 out of 10 accounts, we’ve been able to maintain. And then if you look at the business that’s coming up for grabs, I’d say our win rate here is over 50%.

So when you think about that math, retaining 90% and winning 50% of the new businesses, that’s what ultimately drives our top-line growth. And then once you put those instruments in, then the key aspect here is to be able to expand the menu use of those instruments while they’re in an account, right? You’ve got the capital deployed, you’ve got the service cost that’s kind of been deployed there. So everything we can do to be able to add new menus, new tests, etc., is accretive from both the top and the bottom-line. So that’s a big focus of the team on the R&D side is to be able to expand the menus concurrent to what I would say is this kind of placement strategy that we have with the new systems. So Amulet — on your question on Amulet, listen, I think we continue to capture share.

We estimate that we’re in double-digit share position here in the U.S. Longer-term, I would say, our aspiration is to build a significant share position. The European market is much smaller than the U.S. market. In that market, we have a 50% [Phonetic] share. So I think the key thing here is for us is to — every time you’re a new player coming into the market, you have a different technology, we believe ours is superior, but it’s different in terms of how it gets used, how it gets implanted. So you need to make sure that the physicians as you roll it out, learn how to use our product, our implant, our system, and from there, you build off there. So I think we’ll be looking at not only expansion into new accounts, but also utilization in existing accounts. And that’s the piece that I’m actually getting very excited about it. As we’ve looked at the accounts that we started back in September and October, we’re starting to see nice share movement over there. So that’s very exciting for us. So let me…

Matt Miksic — Credit Suisse — Analyst

That’s great. Thanks so much.

Robert B. Ford — Chairman and Chief Executive Officer

Yeah, let me just close here. I think we’ve had a very strong start to the year, like I said in my prepared comments. We’ve reaffirmed our guidance that we set back in January, absorbing, I would say, impact of the Nutrition recall, which we’re working hard on to restart. Other parts in Nutrition are doing very well, and I expect them to continue to do very well. We’re absorbing, as Bob said, challenges with inflation in the supply chain that many companies I know are facing, and we’re absorbing some headwinds on FX side.

That being said, there’s a lot of great things that are going on at Abbott in the Company, a lot of positives. I talked about them in the beginning of the call. And I’d expect all of that positive to continue and to that momentum to continue to build on that business. Like I said, excluding COVID, excluding some of the recall products, our base business grew 11% in the quarter, and the team is focused on building off that and building off that momentum. So thanks.

Scott Leinenweber — Vice President, Investor Relations

Very good. Thank you, operator, and thank you for all of your questions. This now concludes Abbott’s conference call. A webcast replay of this call will be available after 11 A.M. Central Time today on Abbott’s Investor Relations website at abbottinvestor.com. Thank you for joining us today.

Operator

[Operator Closing Remarks]