ABBOTT LABORATORIES quarterly report, Q3 FY2022

Abbott Laboratories 2022 Q3 Form 10-Q Summary

Business context and reporting period

Abbott Laboratories filed an unaudited Form 10-Q for the quarter and nine months ended September 30, 2022. The company operates through four reportable segments: Established Pharmaceutical Products, Nutritional Products, Diagnostic Products, and Medical Devices. Results are compared with the corresponding 2021 periods.

Key financial metrics

MetricQ3 2022Q3 20219M 20229M 2021
Net sales$10.410B$10.928B$33.562B$31.607B
Operating earnings$1.770B$2.546B$7.058B$6.047B
Net earnings$1.435B$2.100B$5.900B$5.082B
Diluted EPS$0.81$1.17$3.32$2.83
Gross margin50.7%54.8%52.1%51.6%
Operating margin17.0%23.3%21.0%19.1%
Net margin13.8%19.2%17.6%16.1%

Net cash from operating activities was $7.255 billion for the first nine months, down from $7.466 billion in the prior-year period. Capital expenditures were $1.167 billion, dividends paid were $2.486 billion, and share repurchases were $3.110 billion. Cash and cash equivalents were $9.594 billion at September 30, 2022, versus $9.799 billion at December 31, 2021.

Total debt was approximately $16.414 billion at September 30, 2022, compared with $18.050 billion at year-end 2021. Current and long-term debt were $1.117 billion and $15.297 billion, respectively. Abbott reported $5.0 billion of available credit lines expiring in 2025, investment-grade ratings of AA- from S&P and A1 from Moody’s, and approximately $3.116 billion remaining under its 2021 share-repurchase authorization.

Material changes versus prior comparable periods

  • Third-quarter sales declined 4.7% reported but increased 1.3% excluding foreign exchange. The stronger U.S. dollar reduced total sales by 6.0%.
  • Nine-month sales increased 6.2% reported and 10.9% excluding foreign exchange, primarily due to COVID-19 diagnostic testing demand and growth in Medical Devices and Established Pharmaceutical Products.
  • Q3 operating earnings declined 30.5% and net earnings declined 31.7%; diluted EPS fell 30.8%. For the nine months, operating earnings increased 16.7%, net earnings increased 16.1%, and diluted EPS increased 17.3%.
  • Q3 gross margin fell 410 basis points, reflecting the infant-formula recall and Sturgis facility stoppage, WIC-related product prioritization, higher manufacturing and supply-chain costs, lower COVID-19 testing sales, and the nonrecurrence of a favorable 2021 restructuring estimate. Nine-month gross margin improved 50 basis points because of higher rapid-test sales and the nonrecurrence of 2021 restructuring charges.
  • Nine-month Diagnostic Products sales increased 18.9% reported and 23.1% excluding foreign exchange, while Medical Devices sales increased 3.0% reported and 8.4% excluding foreign exchange. Established Pharmaceutical Products increased 5.2% reported, while Nutritional Products declined 9.8%.
  • FreeStyle Libre sales were $3.1 billion for the nine months, up 22.8% excluding foreign exchange. COVID-19 testing-related sales were approximately $7.3 billion, compared with $5.4 billion in the prior-year period.
  • Working capital increased to $11.5 billion from $11.1 billion, primarily because of higher inventories. Inventory increased to $5.734 billion from $5.157 billion at year-end 2021.

Guidance, outlook, commentary, risks, and unusual items

The filing does not provide a clear quantitative earnings or revenue guidance figure. Management stated that the future effects of the COVID-19 pandemic remain uncertain and that inflation, supply-chain disruption, and unfavorable foreign exchange rates could materially affect results.

  • Abbott voluntarily recalled certain infant powder formulas in February 2022 and stopped production at its Sturgis, Michigan facility. Partial production restarted in July 2022 after a May 2022 FDA consent decree. U.S. pediatric nutritional sales declined 31.7% for the first nine months; recalled-brand formula sales were $277 million versus $900 million in the prior-year period.
  • Third-quarter research and development expense included a $111 million impairment charge for certain medical-device in-process R&D intangible assets.
  • The company recorded approximately $172 million of nine-month charges related to the nutritional-product recall and $12 million of restructuring charges. A $13 million restructuring accrual remained at September 30 for the earlier COVID-19 diagnostic manufacturing-network plan, and $34 million remained for other restructuring activities.
  • Remaining performance obligations were approximately $3.9 billion in Diagnostics and $433 million in Medical Devices. Abbott expects to recognize approximately 60% over the next 24 months and 16% over the subsequent 12 months.
  • Legal and environmental proceedings had an estimated possible loss range of approximately $40 million to $50 million, with a recorded accrual of approximately $45 million. Management did not expect these matters to have a material adverse effect, although outcomes remain uncertain.
  • Abbott estimated that gross unrecognized tax benefits could decrease by approximately $75 million to $100 million within the next 12 months as tax matters are resolved.
  • The company declared quarterly dividends of $0.47 per share in each of the first three quarters, up from $0.45 per share in the comparable 2021 periods.

Investor verification checklist

  • Verify the sustainability of revenue and earnings as COVID-19 diagnostic testing demand declines.
  • Track the recovery of U.S. pediatric nutrition sales, the Sturgis facility’s production, recall-related costs, and regulatory compliance.
  • Assess gross-margin effects from inflation, commodities, distribution costs, supply constraints, and product mix.
  • Reconcile reported versus foreign-exchange-adjusted growth, particularly in international markets.
  • Monitor inventory levels and working-capital investment relative to operating cash flow.
  • Review debt maturities, interest-rate exposure, share repurchases, dividend commitments, and remaining liquidity.
  • Evaluate the potential effect of litigation, tax examinations, contingent consideration, restructuring, and intangible-asset impairments.