1,425 pharmaceutical and medication recalls tracked. Stay informed about FDA drug safety alerts, prescription medications, over-the-counter drugs, and dietary supplements.
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Olympus Corporation of the Americas recalled the Thunderbeat, 5 mm, 45 cm, Pistol Grip device on October 22, 2025. The recall affects 30 units distributed worldwide, including the U.S., Canada, Brazil, Germany, Mexico, and Japan. Patients and healthcare providers must stop using this device immediately due to reports of adverse events.
Olympus Corporation of the Americas recalled the Thunderbeat surgical device on October 22, 2025, due to reports of adverse events. The recall affects 30 units distributed worldwide, including the US, Canada, and Japan. Patients and healthcare providers must stop using the device immediately.
Olympus Corporation of the Americas recalled the Thunderbeat 5 mm, 35 cm, Front-Actuated Grip on October 22, 2025. The recall follows reports of adverse events associated with the device. Healthcare providers and patients must stop using this product immediately.
Olympus Corporation of the Americas recalled 9,542 units of the Thunderbeat 5 mm, 45 cm, Front-Actuated Grip Type S on October 22, 2025. The recall follows continued reports of adverse events associated with the device. Patients and healthcare providers must stop using it immediately and follow manufacturer instructions.
Olympus Corporation recalled 3,381 units of the Thunderbeat surgical instrument on October 22, 2025. The recall follows continued reports of adverse events associated with the device. Patients and healthcare providers must stop using the product immediately.
Olympus Corporation of the Americas recalled 88,268 units of the Thunderbeat surgical device on October 22, 2025. The recall follows reports of adverse events associated with the device. Healthcare providers and patients should stop using the device immediately and follow the recall instructions.
Olympus Corporation of the Americas recalled 4,181 units of its Thunderbeat surgical device on October 22, 2025. Reports of adverse events prompted the removal of this device. The recall affects devices distributed worldwide, including the US, Brazil, Canada, Germany, Mexico, and Japan.
Olympus Corporation of the Americas recalled the Thunderbeat 5 mm, 20 cm, Front-Actuated Grip on October 22, 2025. The recall follows ongoing reports of adverse events associated with the medical device. Patients and healthcare providers must stop using the device immediately and follow recall instructions.
Olympus Corporation of the Americas recalled 140 units of its Thunderbeat surgical device on October 22, 2025. Users reported ongoing adverse events linked to the device. Healthcare providers should stop using it immediately and follow recall instructions.
Olympus Corporation of the Americas recalled 1,538 units of the Thunderbeat 5 mm, 10 cm, Inline Grip on October 22, 2025. The recall follows multiple reports of adverse events linked to the device. Healthcare providers and patients should stop using it immediately and follow the manufacturer's instructions.
Olympus Corporation of the Americas recalled 52 units of the Thunderbeat, 5 mm, 35 cm, Inline Grip on October 22, 2025. Reports of adverse events prompted the removal of this medical device from the market. The recall affects distribution in the US, Brazil, Canada, Germany, Mexico, and Japan.
Olympus Corporation of the Americas recalled the Thunderbeat, 5 mm, 45 cm Front-Actuated Grip on October 22, 2025. The recall follows ongoing reports of adverse events associated with the device. Healthcare providers and patients must stop using the instrument immediately.
Medtronic MiniMed recalled 12,126 glucose monitoring devices on October 21, 2025. A software error can lead to incorrect glucose readings, risking hypoglycemia or hyperglycemia. Affected consumers should stop using the device immediately and contact their healthcare provider.
Bristol-Myers Squibb recalled 12,778 vials of Opdualag injection on October 21, 2025. The recall stems from a lack of assurance of sterility. The affected products were distributed nationwide in the United States.
Mindray DS USA, Inc. recalled 54 units of the Isoflurane V90 Electronic Vaporizer on October 20, 2025. The recall stems from a potential anesthesia leakage issue that poses serious health risks. Affected devices were distributed in the U.S. and Canada.
Mindray DS USA, Inc. recalled 148 units of the V90 Electronic Vaporizer on October 20, 2025. The recall follows reports of potential anesthesia leakage that could impact patient safety. Healthcare providers and patients must stop using the device immediately.
Straumann USA recalled 61 units of Emdogain on October 17, 2025. The product, intended for demonstration only, poses a risk if used on patients. Consumers must stop using the affected products immediately.
Beckman Coulter recalled 36,981 bicarbonate reagents on October 14, 2025. The reagent may produce falsely high bicarbonate results due to interference from Lactate Dehydrogenase. Healthcare providers and patients must stop using it immediately.
DermaSensor recalled 343 diagnostic devices on October 13, 2025, due to a risk of incorrect results. The recall affects nine units specifically identified for failing to meet specifications. This issue could delay patient referrals for necessary treatment.
Paragon 28 recalled 20 units of its fibula nail system on October 13, 2025. The recall affects devices with out-of-specification thread depths, risking surgical complications. Patients and healthcare providers must stop using the affected devices immediately.
Gabriel Cosmetics, Inc. recalled 1,617 tubes of Mineral Sunscreen SPF 50 on October 10, 2025, due to CGMP deviations. The affected product contains 21% zinc oxide and is distributed in California, Colorado, Florida, Puerto Rico, and Washington.
Beauty4Pros LLC recalled 1,492 tubes of Karina Daily Moisturizer SPF 25 on October 10, 2025. The recall follows concerns regarding current good manufacturing practice (CGMP) deviations. Affected products were distributed in California, Colorado, Florida, Puerto Rico, and Washington.
Elixir by Coco March recalled tinted mineral sunscreen due to CGMP deviations. The recall affects products distributed in California, Colorado, Florida, Puerto Rico, and Washington. Consumers should stop using the product immediately and seek guidance from healthcare providers.
Sugared+Bronzed recalled 2,090 tubes of Tinted Mineral Sunscreen SPF 50 on October 10, 2025. The recall stems from current Good Manufacturing Practice deviations. Consumers should stop using the product immediately and seek guidance.
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