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Abbott Laboratories: Q3 FY2026 earnings call

What management said about Q3 FY2026, from the documents filed with the SEC on 21 October 2026: press release. Guidance figures: 1 lowered, 1 new, 1 kept. The quarter’s numbers.

Key takeaways

  • Sales grew on both bases: Reported sales rose 14.5 percent to $13.0 billion; comparable growth of 7.0 percent includes Exact Sciences in both periods. Source
  • GAAP EPS fell; adjusted EPS rose: GAAP diluted EPS was $0.53 against $0.94 a year earlier; adjusted diluted EPS, excluding specified items, was $1.42 against $1.30. Source
  • Diagnostics grew with Exact Sciences: Diagnostics sales rose 46.7 percent reported and 6.4 percent comparable; the reported gap reflects the Exact Sciences acquisition. Source
  • Devices grew on comparable basis: Worldwide Medical Devices sales rose 6.9 percent reported and 7.8 percent comparable. Source
  • Libre Duo approved by FDA: The FDA approved Libre Duo in August, a dual glucose-ketone sensor intended to flag rising ketone levels for people with diabetes. Source
  • Gill and NEC settlements charged: Other specified items included about $670 million for agreements resolving the Gill case and NEC claims, covering about 2,000 additional infants. Source

“Abbott delivered strong third-quarter results, reflecting balanced growth across our portfolio,”

Robert B. Ford, chairman and chief executive officer, Abbott

Guidance

AreaPeriodFigureAgainst last quarter
Comparable sales growth SourceFull year 2026approximately 6.0 percentLowered from 6.5% to 7.5%
Adjusted diluted EPS SourceFull year 2026$5.50 to $5.55Kept
Adjusted diluted EPS SourceFourth quarter 2026$1.62 to $1.67New

What changed from last quarter

  • Guidance lowered: Full-year comparable sales growth guidance moved from 6.5 to 7.5 percent to approximately 6.0 percent.
  • Guidance kept: Adjusted EPS guidance midpoint reaffirmed; the range narrowed from $5.45 to $5.60 to $5.50 to $5.55. Source
  • New guidance: Fourth-quarter 2026 adjusted diluted EPS guidance was given in this release. Source
  • New: Libre Duo received FDA approval in August, after the CE Mark announced in May. Source
  • New: SimpleScreen CRC, a blood-based colorectal cancer screening test, was launched in September. Source
  • New: Similac 360 Total Care Made With Whole Milk, a commercially sterile ready-to-feed liquid formula, was launched in August. Source

Results and growth drivers

  • Sales grew on both bases: Reported sales rose 14.5 percent to $13.0 billion; comparable growth of 7.0 percent includes Exact Sciences in both periods. Source
  • GAAP EPS fell; adjusted EPS rose: GAAP diluted EPS was $0.53 against $0.94 a year earlier; adjusted diluted EPS, excluding specified items, was $1.42 against $1.30. Source
  • Operating earnings fell on amortization: Operating earnings were $1,358 million against $2,057 million; amortization of intangible assets was $841 million against $420 million. Source
  • Nine-month adjusted EPS rose: Nine-month adjusted diluted EPS was $3.88 against $3.65; nine-month GAAP diluted EPS was $1.67 against $2.70. Source

Segments and regions

  • Diagnostics grew with Exact Sciences: Diagnostics sales rose 46.7 percent reported and 6.4 percent comparable; the reported gap reflects the Exact Sciences acquisition. Source
  • Cancer Diagnostics led by Cologuard: Cancer Diagnostics growth was driven by Cologuard, with contributions from precision oncology and international businesses. Source
  • Devices grew on comparable basis: Worldwide Medical Devices sales rose 6.9 percent reported and 7.8 percent comparable. Source
  • Electrophysiology and rhythm management double-digit: Double-digit growth in Electrophysiology and Rhythm Management led device sales growth in the quarter. Source
  • Nutrition grew, pediatric near nine percent: Nutrition sales rose 5.1 percent reported and 4.9 percent comparable; Pediatric sales grew nearly 9.0 percent. Source
  • Emerging markets drove branded generics growth: Key Emerging Markets sales rose 10.9 percent comparable, led by double-digit growth in India and several Latin America and Asia Pacific markets. Source

“With strong performance across multiple businesses and a robust pipeline of innovation, we are well-positioned to deliver sustainable growth in the years ahead.”

Robert B. Ford, chairman and chief executive officer, Abbott

Product approvals and launches

  • Libre Duo approved by FDA: The FDA approved Libre Duo in August, a dual glucose-ketone sensor intended to flag rising ketone levels for people with diabetes. Source
  • TactiFlex Duo catheter approved by FDA: The FDA approved the TactiFlex Duo Ablation Catheter in September, combining pulsed field ablation and radiofrequency energy. Source
  • SimpleScreen CRC test launched: The blood-based colorectal screening test was launched in September for adults age 45 and older at average risk. Source
  • Amulet 360 received CE Mark: The Amulet 360 left atrial appendage occluder received CE Mark in August; the prior release reported its FDA submission in May. Source
  • Similac 360 whole-milk formula launched: Similac 360 Total Care Made With Whole Milk was launched in August as a commercially sterile, ready-to-feed liquid formula. Source

Costs, margins and pricing

  • Gross margin reported and adjusted: Gross margin after intangible amortization was $6,544 million, or $7,448 million excluding specified items. Source
  • SG&A rose 39.8 percent: Selling, general and administrative expense rose to $4,266 million, with specified SG&A items of $761 million. Source
  • R&D spending rose 20.1 percent: Research and development expense rose to $920 million from $766 million a year earlier. Source
  • Reported tax rate was 25.3 percent: The reported tax rate for the quarter was 25.3 percent on pre-tax earnings of $1,231 million. Source

Legal and regulatory charges

  • Gill and NEC settlements charged: Other specified items included about $670 million for agreements resolving the Gill case and NEC claims, covering about 2,000 additional infants. Source
  • Nine-month DOJ agreement charge: Nine-month specified items included about $400 million, with fees and interest, to resolve DOJ investigations and a qui tam lawsuit. Source

Capital, cash and shareholder returns

  • Quarterly dividend of $0.63 declared: The board declared a quarterly dividend of $0.63 per share on September 17, 2026. Source
  • Dividend raised 54 consecutive years: Management said Abbott has increased its dividend payout for 54 consecutive years and is an S&P 500 Dividend Aristocrat. Source
  • Interest expense rose to $297 million: Net interest expense was $297 million in the quarter against $44 million a year earlier. Source
  • Average share count slightly lower: Average shares outstanding including dilutive options were 1,738 million against 1,749 million a year earlier. Source

Strategy, reporting changes and acquisitions

  • Exact Sciences now in Cancer Diagnostics: Abbott completed the Exact Sciences acquisition on March 23, 2026; its sales are reported within Cancer Diagnostics. Source
  • Amulet moved to Electrophysiology: The Amulet occluder and related accessories moved from Structural Heart to Electrophysiology on January 1, 2026, with prior-year sales reclassified. Source
  • Structural Heart compensation payments ended: Comparable sales exclude the compensation payments from a multi-year competitor agreement; the final payment was recognized in the first quarter. Source

Coming up, as management said on 21 October 2026

  • Quarterly dividend payable November 16: The $0.63 cash dividend is payable on November 16, 2026, to holders of record at the close of business on October 15, 2026. Source

Figures management reported

FigureReported
Established Pharmaceuticals sales Source$1,614 million; 6.8 percent reported and 8.4 percent comparable growth
Research and development expense Source$920 million, up 20.1 percent
Cologuard and cancer diagnostics SourceCancer Diagnostics sales of $968 million; Cologuard growth cited without a separate figure
Continuous glucose monitor sales Source7.3 percent reported and 7.7 percent comparable growth
Pipeline milestones SourceOne CE Mark, two FDA approvals and two product launches announced in the quarter

Risks management discussed

  • Financial: Abbott does not give GAAP guidance because restructuring, impairments, acquisition costs and foreign exchange could significantly affect GAAP results. Source
  • Regulatory: Incremental costs to comply with EU device rules for previously approved products are included in specified items. Source

Earlier plans management reported on

  • Not stated: The prior release expected momentum to drive accelerating growth in the second half; this release does not restate that expectation.
  • Not stated: The prior release projected third-quarter adjusted diluted EPS; this release does not state whether that projection was met.
  • Not stated: Management reaffirmed the midpoint of the prior full-year adjusted EPS range and tightened the range. Source

Other quarters

Summarised with AI from the documents the company filed with the SEC. Every point is checked against the filing before it is shown: management’s own words word for word, figures against the line or table row they come from. A point that fails the check is left out. Source opens the filing at that line.