Fourth-quarter and full-year 2025 results | Adjusted diluted EPS | | | | --- | --- | --- | | Fourth quarter | $1.501 | ↑12% | | Full year | $5.152 | % ↑10 | | W orldwide sales | Organic* sales growth for underlying base business** | 5 Full-year 2026 guidance | | $11.5B | ↑3.8%3 | 6.5% to 7.5% | | Fourth quarter | | Organic sales growth | | $44.3B | ↑6.7%4 | $5.55 to $5.80 | | Full year | | Adjusted diluted EPS | Key business units | Fourth-quarter sales Expanding in the fast-growing pulsed field ablation (P ...

Core Insights - Abbott reported strong financial results for Q4 2025, with total worldwide sales reaching $11.459 billion, a 4.4% increase from Q4 2024 [28] - The company achieved double-digit earnings per share growth, with adjusted diluted EPS of $1.50, reflecting a 12% increase [5] - Abbott's full-year 2025 sales totaled $44.328 billion, marking a 5.7% increase compared to 2024 [28] Financial Performance - Q4 2025 sales increased 4.4% on a reported basis and 3.0% on an organic basis, with a 3.8% increase when excluding COVID-19 testing-related sales [5][28] - Full-year 2025 GAAP diluted EPS was $3.72, while adjusted diluted EPS was $5.15, reflecting a 10% growth [5][28] - Abbott projects full-year 2026 organic sales growth to be in the range of 6.5% to 7.5% and adjusted diluted EPS of $5.55 to $5.80 [5][22] Segment Performance - In Q4 2025, Nutrition sales decreased by 8.9% on a reported basis and 9.1% on an organic basis, primarily due to lower sales volumes [9][10] - Diagnostics sales in Q4 2025 were $2.457 billion, a decrease of 2.5% on a reported basis and 3.6% on an organic basis [12][28] - Medical Devices sales increased by 12.3% on a reported basis and 10.4% on an organic basis, driven by strong growth in Electrophysiology and Diabetes Care [19][20] Strategic Developments - Abbott announced an agreement to acquire Exact Sciences, positioning the company to enter the cancer diagnostics market [5] - The company received FDA approval for its Volt™ PFA System and CE Mark for its TactiFlex™ Duo Ablation Catheter, enhancing its Electrophysiology portfolio [5][10] Dividend Information - Abbott declared a quarterly dividend of $0.63 per share, marking the 408th consecutive quarterly dividend and reflecting a commitment to returning value to shareholders [24]

Earnings Report - Abbott Laboratories is set to release its fourth-quarter earnings on January 22, with expected earnings of $1.49 per share, an increase from $1.34 per share in the same period last year [1] - The consensus estimate for Abbott's quarterly revenue is $11.8 billion, up from $10.97 billion reported last year [1] Recent Developments - On January 20, Abbott received CE Mark approval for the TactiFlex™ Duo Ablation Catheter, aimed at treating patients with abnormal heart rhythms [2] - Following this news, Abbott's shares fell by 0.3%, closing at $120.73 [2] Analyst Ratings - Bernstein analyst Lee Hambright maintained an Outperform rating and raised the price target from $150 to $154 [3] - Barclays analyst Matt Miksic maintained an Overweight rating and increased the price target from $162 to $169 [3] - BTIG analyst Marie Thibault maintained a Buy rating with a price target of $145 [3] - Raymond James analyst Jayson Bedford maintained an Outperform rating and raised the price target from $141 to $146 [3] - Evercore ISI Group analyst Vijay Kumar maintained an Outperform rating but reduced the price target from $144 to $142 [3]

Core Viewpoint - Abbott has received CE Mark approval for the TactiFlex™ Duo Ablation Catheter, which is designed to treat patients with atrial fibrillation (AFib) in Europe, marking a significant advancement in cardiac ablation technology [1][4]. Product Overview - The TactiFlex Duo Catheter utilizes pulsed field ablation (PFA) technology and offers dual options for treatment: radiofrequency energy and pulsed field ablation energy, allowing for tailored therapy lesions [2][8]. - This catheter is designed to improve the effectiveness of cardiac ablation procedures by minimizing damage to adjacent tissues, particularly in patients with complex disease or anatomy [2][6]. Clinical Significance - Approximately eight million Europeans over the age of 65 are living with AFib, a number expected to double in the next 30 years, highlighting the growing need for effective treatment options [5]. - Successful cardiac ablation can significantly reduce the risk of AFib recurrence and improve patients' quality of life, especially for those who do not respond to traditional treatments [3][6]. Regulatory Progress - The TactiFlex Duo represents the third major approval in Abbott's electrophysiology portfolio within a year, following the Volt PFA System's approvals in 2025 [7]. - The CE Mark approval was supported by data from the FOCALFLEX CE Mark study, which demonstrated the catheter's safety and effectiveness in treating AFib [4]. Integration with Existing Technology - TactiFlex Duo integrates with Abbott's EnSite™ X EP System, which provides detailed three-dimensional mapping of the heart, enhancing the precision of arrhythmia treatment [6]. - This integration allows for a more comprehensive approach to patient care, enabling physicians to utilize multiple clinically proven tools for a wide range of arrhythmias [9].