1,817 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.
FDA recalls READYPREP PVP, povodone-iodine 10% topical antiseptic. Medline Industries issued the nationwide recall. Subpotent drug is the reason. Consumers should stop using the product immediately.
Boston Scientific recalled 19 ICEfx Cryoablation System units worldwide, including the United States, Canada, France, Germany and Italy. The recall concerns desiccant tube subassemblies with end caps that were not tightened. Clinicians and patients should stop using the device immediately and follow recall instructions issued by the manufacturer.
Boston Scientific recalled 1 unit of the Preventive Maintenance Kit SPRPM8000 after certain desiccant tubes were built with incorrectly tightened end caps. This assembly defect can lead to device malfunction, posing a serious risk to patients. Healthcare providers and patients should stop using the device immediately and follow recall instructions from the manufacturer.
Amneal Pharmaceuticals products containing chlorpromazine hydrochloride are recalled nationwide after the FDA-linked notice identifies a foreign substance in packaging material. No tablets were contaminated. The recall was issued August 18, 2025 and updated September 10, 2025. Consumers and healthcare providers should stop using the affected lots immediately and contact Amneal for guidance.
Amneal Pharmaceuticals recalled 13,130 bottles of CHLORPROMAZINE HYDROCHLORIDE 50 mg tablets distributed nationwide in the USA. A specific lot of auxiliary polyester coil used in packaging was found to contain a microorganism. No microorganism was detected on any tablets. Consumers and healthcare providers should stop using this product immediately and await further instructions from Amneal or a H
B. Braun Medical Inc. recalls 47,148 containers of 0.9% Sodium Chloride Injection USP nationwide after detecting particulate matter. The Class I recall affects bottles with NDC 0264-7800-09. Stop using and contact providers for guidance.
Amneal Pharmaceuticals LLC is recalling 7,228 bottles of CHLORPROMAZINE HYDROCHLORIDE tablets sold nationwide in the United States. Packaging coils used in the bottles tested positive for a microorganism, though no tablets were contaminated. Stop using this product immediately and contact Amneal or your healthcare provider for guidance.
Amneal Pharmaceuticals recalled 60,072 100-count bottles and 73,054 500-count bottles of sulfamethoxazole and trimethoprim tablets. A foreign packaging material was detected in a lot, with no tablets contaminated. The recall is nationwide and ongoing as of the report date.
B. Braun Medical recalled 46,032 containers of Lactated Ringers Injection USP sold nationwide in the United States. The recall cites the presence of particulate matter in the 1000 mL IV solution. Consumers should stop using the product immediately and contact their healthcare provider or B. Braun for guidance.
Amneal Pharmaceuticals recalled 14,923 bottles of Chlorpromazine Hydrochloride 100 mg tablets sold nationwide in the United States. A packaging coil used in the product’s packaging was found to contain a microorganism. No microorganism was detected on any tablets. Stop using the product and contact Amneal or your healthcare provider for guidance.
CorNeat Vision recalled 630 EverPatch surgical matrices distributed worldwide, including in 28 U.S. states. Review of complaints found conjunctival wound dehiscence may lead to early exposure of the patch. Stop using the device immediately and follow the manufacturer’s recall instructions. Contact CORNEAT VISION, LTD. or your healthcare provider for guidance.
Aesculap AG recalls the ELAN 4 Fixed Duraguard Long device, Model GB943R, after mislabeling errors were discovered. The U.S. distribution reached Missouri with international distribution to multiple countries. Healthcare providers should stop using the device immediately per manufacturer instructions.
CORNEAT VISION recalled 180 units of EverPatch+ scleral reinforcement patch worldwide after complaints of conjunctival wound dehiscence. The issue can lead to early exposure of the surgical patch. Clinicians and patients should stop using the device immediately and follow the manufacturer recall instructions.
Aesculap AG is recalling one unit of the ELAN 4 Fixed Duraguard Standard, model GB942R, distributed in the United States to Missouri and internationally to multiple countries. The recall addresses mislabeling where the Standard was labeled as Long and the Long was labeled as Standard. Patients and healthcare providers should stop using this device immediately and follow the manufacturer’s recall指南
Maquet Cardiovascular recalled 16,512 Heartstring III Proximal Seal Systems due to three identified failure modes. The device may fail to load, deploy, or provide adequate hemostasis during use. Healthcare providers must stop using the device immediately and contact the manufacturer for guidance.
Exactech recalled 11,542 Equinoxe reverse shoulder humeral liners worldwide after finding the articular surface position outside labeling specifications. The recall covers several REF numbers and UDIs and is active as of 2025. Healthcare providers were advised to stop using affected liners and follow manufacturer instructions.
Exactech recalled 61,334 Equinoxe reverse shoulder humeral liners sold worldwide after finding the articular surface position outside labeling dimensions. The recall covers REF 320-38-00, REF 320-38-03, REF 320-42-00, and REF 320-42-03. Healthcare providers and patients should stop using the devices immediately and follow recall instructions distributed by email.
Ethicon recalled 516 STRATAFIX Spiral PDS Plus Bidirectional Knotless Tissue Control Devices sold worldwide through healthcare providers, including 18 U.S. states and Singapore and Malaysia. The defect is potential barb non-engagement that could compromise tissue control. Clinicians and patients should stop using the device immediately and follow recall instructions from Ethicon.
Mindray DS USA, Inc. dba Mindray North America recalled 2,278 BeneVision N1 patient monitors distributed worldwide, including Canada. The devices may activate an abnormal alarm pause. Hospitals and clinicians should stop using the devices immediately and follow the recall instructions issued by Mindray.
Maquet Cardiovascular recalled 168 Heartstring III Proximal Seal System intravascular occluders worldwide, including the United States. Three failure modes have been identified: loading the Heartstring Seal, deploying it into the aortotomy, and achieving adequate hemostasis. Healthcare facilities should stop using the device and follow the manufacturer’s recall instructions.
Maquet Cardiovascular recalls the Heartstring III Proximal Seal System, a 3.8 mm intravascular anastomosis occluder used by hospitals worldwide. Three failure modes have been identified: loading failure, deployment failure, and failure to provide adequate hemostasis. Healthcare facilities should stop using the device immediately and follow manufacturer recall instructions.
Drinkmate recalled certain 1-liter carbonation bottles after receiving reports of potential explosions. Users may suffer serious laceration and hearing damage from exploding bottles. Consumers should stop using the bottles immediately and contact Drinkmate for a free replacement.
Firefly Fuel Inc. recalled Firefly Safe & Green 32 oz. bottles. The recall date is August 14, 2025. The fuel is sold in a clear bottle with a white cap and nozzle applicator. The product label shows Firefly brand, Safe & Green in green font, and claims Non-Toxic and Kosher. The nozzle applicator lacks child-resistant features, violating the Poison Prevention Packaging Act and the Federal Hazardous
Philips North America LLC is recalling 181 CT systems worldwide, including Brilliance CT 40 Channel 728235, Brilliance CT 64 Channel 728231, and Ingenuity Flex 728317. The patient support couch may descend to the lowermost position after a replacement. Hospitals and imaging centers should stop using the devices immediately and await recall instructions.
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