1,894 pharmaceutical and medication recalls tracked. Stay informed about FDA drug safety alerts, prescription medications, over-the-counter drugs, and dietary supplements.
Looking for a specific drug? Use the search page to find recalls by medication name, manufacturer, or NDC number.
Sheathing Technologies recalled 12 units of its ultrasound probe covers on November 17, 2025, due to potential contamination risks. The non-sterile vaginal and rectal covers may have defects that pose an infection risk during use. Consumers should stop using the product immediately and follow the manufacturer's instructions.
Intuitive Surgical recalled 12 Da Vinci 5 surgical consoles on November 17, 2025. A software error may cause loss of user interface content on external monitors. Healthcare providers must stop using the devices immediately.
ETAC A/S recalled 64 units of Molift 2-point sling bars on November 17, 2025. A defect in the mounting bolt can lead to failure during use. This poses serious risks for users relying on the device for mobility assistance.
Molift recalled 71 Mover 300 mobile hoists on November 17, 2025, due to a potential bolt failure. The defect can lead to limited mobility, posing a high risk to users. Affected models include M1501, M1502, M1504, among others.
Cipla USA recalled 12,576 bottles of Cinacalcet Hydrochloride Tablets on November 14, 2025, due to a nitrosamine impurity. The impurity, N-nitroso-cinacalcet, exceeds acceptable daily intake limits. Consumers must stop using this product immediately and contact healthcare providers for guidance.
Cipla USA, Inc. recalled 63,504 bottles of Cinacalcet Hydrochloride Tablets on November 14, 2025. The recall results from a nitrosamine impurity, N-nitroso-cinacalcet, exceeding acceptable daily intake limits. Consumers should stop using the tablets immediately and contact healthcare providers for guidance.
Olympus Corporation of the Americas is recalling 1,082 ShockPulse Lithotripsy System SPL-S single-use probes worldwide. Investigations found the device’s generator may blink and fail to recognize the transducer, risking damage to the transducer plug or generator receptacle. Hospitals and clinics should stop using the device immediately and follow the recall instructions from Olympus.
Olympus Corporation of the Americas recalls 602 ShockPulse-SE Lithotripsy System reusable probes worldwide to hospitals. The recall cites a blinking generator that may fail to recognize the transducer and damage the transducer plug or generator receptacle. Hospitals and patients should stop using SPL-SR probes immediately and follow manufacturer recall instructions.
Olympus Corporation of the Americas is recalling 1,684 ShockPulse-SE Lithotripsy System generators worldwide, including SPL-G models. Investigations found the generator can blink and fail to recognize the transducer, and damage to the transducer plug or generator receptacle may occur. Healthcare providers and patients should stop using the device immediately and follow recall instructions provided
Cipla USA, Inc. recalled 15,744 bottles of Cinacalcet Hydrochloride Tablets on November 14, 2025. The recall follows the discovery of a nitrosamine impurity exceeding acceptable daily intake limits. Consumers should stop using the product immediately and consult healthcare providers.
Lupin Pharmaceuticals recalled 32,736 vials of Ganirelix Acetate Injection on November 13, 2025. The recall follows the discovery of impurities in the drug. Consumers and healthcare providers should stop using the product immediately to avoid health risks.
Microbiologics recalled 5 KWIK-STIK quality control kits for culture media after发现 some kits labeled for lot 818-111-7 were packed in pouches marked as lot 857-53-10. The mislabeling could affect quality control results for Vibrio parahaemolyticus tests derived from ATCC 17802. Laboratories and healthcare facilities should stop using the kit and follow the manufacturer’s recall instructions.
Walgreens Saline Nasal Spray With Xylitol, distributed by Walgreens Co., is recalled nationwide. The product was found with microbial contamination, specifically Pseudomonas lactis, in a non-sterile formulation. Consumers should stop using the product immediately and contact Medical Products Laboratories, Inc. for guidance or consult a clinician.
Cardinal Health 200 recalled 251,165 ChemoPlus gowns on November 12, 2025, due to incorrect expiration dates. The gowns are mislabeled with a five-year shelf life instead of the correct three years. Patients and healthcare providers must stop using these gowns immediately.
Stryker recalled 320 units of the CranialMask Tracker on November 12, 2025, due to software errors during surgery. The device fails to activate properly, displaying an error message that prevents its use. Healthcare providers must stop using this device and follow recall instructions immediately.
AVID Medical recalled 52 units of the ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17, on November 11, 2025. The devices are unsuitable for organ transplant procedures, presenting a serious health risk. Healthcare providers must stop using the device immediately and follow recall instructions.
AVID Medical recalled 380 units of the Halyard MINI PLUS KIT SOUTH on November 11, 2025. The devices are unsuitable for organ transplant procedures, posing potential health risks. Healthcare providers and patients must stop using the device immediately.
Medline Industries recalled 163 DEXLOCK Achilles Repair Implant Kits on November 11, 2025, due to a potential hazard. Users reported drill bits fusing to the drill guide, which may prolong surgical procedures. The recall affects kits distributed nationwide in multiple states.
AVID Medical recalled 132 units of its Organ Recovery Kit on November 11, 2025. The devices are not suitable for organ transplant, posing a high risk to patients. Healthcare providers and patients should stop using the device immediately and follow recall instructions.
Olympus recalled 94 units of its 10 Fr. endoscopic sheath on November 11, 2025, due to complaints of the ceramic tip breaking. The defect poses a high risk for patients undergoing urological procedures. Healthcare providers and patients must stop using the device immediately.
Olympus Corporation of the Americas recalled 118 units of its 28 Fr. resection sheath on November 11, 2025. The recall follows reports of the ceramic tip breaking, posing a risk of injury. Healthcare providers and patients must stop using the device immediately.
Olympus Corporation of the Americas recalled the Inner Sheath Model No. A2641 on November 11, 2025. The recall follows complaints of the ceramic tip breaking, posing a high risk of injury to patients. Healthcare providers and patients should stop using the device immediately and follow recall instructions.
Olympus Corporation of the Americas recalled 437 units of the Inner Sheath, Model No. WA22017A, on November 11, 2025. The recall follows complaints of the ceramic tip breaking during use, posing a significant risk to patients. Healthcare providers and patients should cease use immediately and follow the manufacturer’s instructions.
Olympus Corporation of the Americas recalled 6,949 units of its Resection Inner Sheath on November 11, 2025, after reports of the ceramic tip breaking. This device, used in urologic applications, poses a high hazard risk. Healthcare providers and patients should stop using the device immediately.
Receive immediate notifications when medications you care about are recalled. Stay safe with timely FDA drug safety alerts.