1,355 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.
Spacelabs Healthcare recalled 16,898 DVI display cables on September 5, 2025. The cables may not comply with electromagnetic interference standards, posing risks to patient safety. Healthcare providers and patients must stop using these cables immediately.
Par Pharmaceutical recalled 1,041 cartons of Everolimus tablets on September 5, 2025. The recall stems from failed impurities and degradation specifications. Consumers should stop using the product immediately.
GE Medical Systems recalled 7,302 AW Server units on September 5, 2025, due to a critical security vulnerability. The flaw could allow unauthorized access to sensitive patient data. Healthcare providers and patients must cease use immediately and follow recall procedures.
Apotex Corp. recalled 493,468 bottles of Ketorolac Tromethamine Ophthalmic Solution on September 5, 2025. The recall stems from a lack of assurance of sterility due to improper bottle sealing. Consumers should stop using the product immediately and contact their healthcare provider for guidance.
Spacelabs Healthcare recalled 820 DVI display cables on September 5, 2025. The cables may interfere with other medical devices due to inadequate shielding. Patients and healthcare providers should stop using these cables immediately.
Apotex Inc. recalled 151,034 bottles of Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution on September 5, 2025. The recall stems from a lack of assurance of sterility due to improper bottle sealing. Consumers should stop using the product immediately and contact their healthcare provider or Apotex Corp.
Spacelabs Healthcare recalled 8,179 DVI display cables on September 5, 2025, due to electromagnetic interference issues. The cables can interfere with sensitive medical devices, posing serious safety risks. Patients and healthcare providers must stop using the product immediately.
GE Healthcare recalled 173 units of the Carescape Central Station on September 5, 2025. The device may enter a continuous reboot cycle, risking loss of patient monitoring. This issue occurs when 118 to 120 stations connect to the network.
GE Healthcare recalled 2,306 Carescape Central Station devices on September 5, 2025, due to a software issue. The problem can cause a continuous reboot cycle, risking loss of patient monitoring. The recall affects devices with software version V3.0.5 when connected in specific network conditions.
Zydus Pharmaceuticals recalled 4,440 bottles of Entecavir Tablets on September 4, 2025. The recall follows failure to meet impurity and degradation specifications. Consumers should stop using the affected tablets immediately and contact their healthcare provider.
Zydus Pharmaceuticals recalled 4,344 bottles of Entecavir Tablets on September 4, 2025. The recall stems from failed impurity and degradation specifications. Consumers should stop using the product immediately.
American Contract Systems recalled 32,433 medical convenience kits on September 4, 2025. The products failed to meet sterilization standards, posing a safety risk. Healthcare providers and patients must stop using these kits immediately.
American Contract Systems recalled 32,433 medical convenience kits on September 4, 2025. The recall affects various models due to improper sterilization processes. Patients and healthcare providers must stop using these products immediately.
American Contract Systems recalled 32,433 medical convenience kits after multiple sterilization cycles compromised product safety. The recall, announced on September 4, 2025, stems from nonconformance during Ethylene Oxide gas sterilization. Affected products include kits used for cataract and eye procedures.
American Contract Systems recalled 32,433 medical convenience kits on September 4, 2025, after discovering re-gassing issues. The affected products have not been validated for safety and effectiveness after multiple sterilization cycles.
American Contract Systems recalled 32,433 medical convenience kits on September 4, 2025. These kits failed to meet safety standards due to improper sterilization processes. The recall affects multiple states, including South Dakota and Iowa.
American Contract Systems recalled 32,433 medical convenience kits on September 4, 2025. The recall follows issues with multiple sterilization cycles that compromise product safety. Patients and healthcare providers should stop using these devices immediately.
American Contract Systems recalled 32,433 medical convenience kits on September 4, 2025. The recall follows the identification of products that were re-gassed after sterilization failures. The safety and effectiveness of these products cannot be confirmed due to multiple sterilization cycles.
American Contract Systems recalled 32,433 medical convenience kits on September 4, 2025. The products failed to meet sterilization standards after being re-gassed improperly. Health providers and patients must stop using these devices immediately.
American Contract Systems recalled 32,433 radiology packs on September 4, 2025, due to improper sterilization. The products were re-gassed after a nonconformance in the initial Ethylene Oxide gas injection process. Their safety and effectiveness remain unverified after multiple sterilization cycles.
American Contract Systems recalled 32,433 medical convenience kits on September 4, 2025. The recall stems from products being re-gassed after a nonconformance during sterilization. This compromises the quality and safety of the devices.
American Contract Systems recalled 32,433 Basic Biopsy Trays on September 4, 2025. The recall resulted from products being re-gassed after a sterilization failure. The company cannot confirm the safety or effectiveness of these devices after multiple sterilization cycles.
American Contract Systems recalled 32,433 biopsy trays on September 4, 2025. The recall affects multiple models due to improper re-sterilization that raises safety concerns. Healthcare providers and patients must stop using these products immediately.
American Contract Systems recalled 32,433 medical convenience kits on September 4, 2025, due to improper sterilization. The affected products were re-gassed and not validated for safety after multiple sterilization cycles. Distribution occurred nationwide, including states such as South Dakota and Illinois.
Receive immediate notifications when medications you care about are recalled. Stay safe with timely FDA drug safety alerts.