Browse through 1,551 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Werner Paddles recalled Stealth and Covert kayak paddles on October 30, 2025. The paddles can break during use, creating a drowning hazard. Consumers should stop using the paddles and seek a refund immediately.
Olympus Corporation of the Americas recalled 7,803 units of the HX-400U-30 ligating device on October 30, 2025. The device may fail to release as intended, posing significant risks to patients. Healthcare providers must stop using the device immediately and follow recall instructions.
B Braun Medical recalled 2,100 IV administration sets on October 29, 2025. The recall follows reports of backflow of medication from secondary IV containers into primary IV containers. This poses a high risk for patients using the Infusomat Space, Outlook, and Vista pumps.
B Braun Medical recalled 10,536 Anesthesia IV Sets on October 29, 2025. The recall stems from a risk of medication backflow between IV containers. Healthcare providers must stop using the product immediately to prevent potential harm.
B Braun Medical recalled 32,500 IV extension sets on October 29, 2025. The recall stems from a risk of medication backflow from secondary IV containers. Patients and healthcare providers must stop using the devices immediately.
B Braun Medical recalled 23,160 IV administration sets on October 29, 2025. The sets pose a high risk of medication backflow from secondary containers into primary containers. Healthcare providers should stop using the devices immediately.
B Braun Medical recalled 65,904 IV administration sets on October 29, 2025, due to a risk of backflow from secondary IV containers. This could lead to medication errors that may endanger patients. The sets are used with several pumps, including the Infusomat Space and Outlook Pump.
B Braun Medical recalled 104,784 Anesthesia IV Sets on October 29, 2025. The recall affects models utilized with Infusomat Space, Outlook, and Vista pumps due to potential medication backflow. This hazard poses serious risks for patients receiving IV medication.
B Braun Medical recalled 28,344 IV administration sets on October 29, 2025. The recall affects gravity and pump administration sets used with Infusomat Space, Outlook, and Vista Basic pumps. Users face a high risk of medication backflow into primary IV containers.
B Braun Medical recalled 129,480 IV administration sets on October 29, 2025. The recall follows reports of potential backflow of medication from secondary IV containers into primary containers. Patients and healthcare providers must stop using the devices immediately.
Nate's Fine Foods recalled 972 cases of cooked linguine pasta on September 25, 2025. The recall follows potential contamination with Listeria monocytogenes. Consumers in CA, IN, PA, and TX should not consume the product.
B Braun Medical recalled 24,624 blood administration sets on October 29, 2025, due to a risk of backflow from secondary IV containers. These sets are incompatible with the Infusomat Space, Outlook, and Vista Basic pumps. Healthcare providers must stop using these devices immediately to prevent potential medication errors.
B Braun Medical recalled 7,344 blood administration sets on October 29, 2025. The recall follows a potential backflow hazard that could affect patient safety. Healthcare providers must stop using the affected devices immediately.
B Braun Medical recalled 554,015 IV administration sets on October 29, 2025. The recall addresses a high risk of medication backflow into primary IV containers. Patients and healthcare providers must stop using these sets immediately.
B Braun Medical recalled 48 IV Administration Sets on October 29, 2025, after reports of potential medication backflow. The affected sets are used with the Infusomat Space, Outlook, and Vista Basic Pumps. Healthcare providers must stop using the devices immediately and follow recall instructions.
B Braun Medical recalled over 49 million IV administration sets on October 29, 2025. The recall addresses a potential backflow of medication from secondary IV containers into primary IV containers. Users should stop using the affected devices immediately.
B Braun Medical recalled 135,000 IV administration sets on October 29, 2025. The recall follows reports of potential backflow of medication from secondary IV containers. Healthcare providers must stop using the device immediately.
B Braun Medical recalled 126,050 IV administration sets on October 29, 2025. The recall affects devices used with the Infusomat Space, Outlook, and Vista pumps. Users face a high risk of medication backflow and occlusions.
B Braun Medical recalled 33,528 blood administration sets on October 29, 2025. The recall affects sets used with Infusomat Space, Outlook, and Vista Basic Pumps. The devices pose a backflow risk that could compromise patient safety.
B Braun Medical recalled 11,800 IV extension sets on October 29, 2025. The recall follows reports of potential medication backflow from secondary IV containers. Healthcare providers should stop using the device immediately.