Browse through 1,551 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
B Braun Medical recalled 122,232 IV administration sets on October 29, 2025. The recall addresses potential backflow of medication from secondary IV containers into primary containers. Affected units were distributed worldwide including the US, Canada, Germany, Guatemala, and Singapore.
B Braun Medical recalled 66,792 IV Administration Sets on October 29, 2025, due to a potential backflow risk. The recall affects models used with Infusomat Space, Outlook, and Vista Basic Pumps. Healthcare providers must stop using these devices immediately.
B Braun Medical recalled 3,120 IV administration sets on October 29, 2025, due to a risk of medication backflow. The recall affects models used with Infusomat Space, Outlook, and Vista Basic Pumps. The company advises patients and healthcare providers to stop using the devices immediately.
B Braun Medical recalled 150,664 IV administration sets on October 29, 2025. The recall affects products identified by catalog number 375258. These devices pose a high risk of medication backflow from secondary IV containers.
B Braun Medical recalled 19,320 Anesthesia IV Sets on October 29, 2025. The recall follows reports of potential backflow of medication from secondary IV containers. Patients and healthcare providers must stop using the device immediately.
B Braun Medical recalled 18,072 IV administration sets on October 29, 2025. The recall affects the Outlook set utilized with Infusomat Space and Outlook Pumps. The sets pose a high risk of medication backflow and priming issues.
Medtronic recalled 6,591 extravascular implantable cardioverter defibrillators on October 29, 2025. The recall stems from a potential delay in high-voltage therapy that could occur under rare conditions. Patients must stop using the devices immediately and follow manufacturer instructions.
Philips North America recalled six units of the Incisive CT scanner on October 29, 2025, due to a serious safety hazard. The screws on the tube heat exchanger may not be properly tightened, leading to potential detachment during operation. This defect could cause damage to other components within the system.
Philips North America recalled 2,341 Incisive CT scanners on October 29, 2025. A component may detach and damage other parts during operation. Users must stop using the device immediately and follow recall instructions.
Avion Pharmaceuticals recalled 804 bottles of Prenate Chewable vitamins on October 29, 2025, due to undeclared soy. The recall affects consumers in 15 states, including California and Texas. The product also contains a labeling error regarding the amount of boron.
Baxter Healthcare recalled 118 units of the Welch Allyn INF BAG, Model REF 5089-18, on October 28, 2025. The replacement bladder may contain a Large Adult size bladder instead of a Thigh size bladder. This defect poses a high risk for inaccurate blood pressure readings.
Illumina recalled 11,916 NextSeq 550Dx reagent kits on October 28, 2025. Flow cell gaskets in these kits may leak during DNA sequencing runs, risking toxic exposure to users. Healthcare providers must stop using these devices immediately and follow recall instructions.
Moonlight Packing Corporation recalled 439 bags of Peppermint Peach on October 28, 2025, due to potential Listeria monocytogenes contamination. The affected product weighs 2.25 lbs and may pose a serious health risk to consumers. The recall includes products distributed across multiple states and internationally.
Moonlight Packing Corporation recalled 13,069 cases of white peaches on October 28, 2025. The recall stems from potential contamination with Listeria monocytogenes. Consumers should not eat the recalled peaches and should seek refunds.
Moonlight Packing Corporation recalled 2,622 cases of sticker labels for loose bulk peppermint peaches on October 28, 2025. The recall stems from potential contamination with Listeria monocytogenes. Consumers should not consume this product and should contact the company for a refund or replacement.
Moonlight Packing Corp. recalled 46,048 cases of peaches on October 28, 2025. The recall stems from potential contamination with Listeria monocytogenes. Consumers should not eat the affected product and should seek a refund.
India's Fine Foods recalled 8 pieces of cookware on October 28, 2025, due to potential lead contamination. The affected products could pose a serious health risk to consumers. The recall affects products distributed in California and Washington.
India's Fine Foods recalled 9 pieces of cookware on October 28, 2025, due to potential lead contamination. Consumers should not use these products and can contact the company for refunds or replacements.
Moonlight Packing Corporation recalled 104 cases of white peaches on October 28, 2025, due to potential contamination with Listeria monocytogenes. The recall affects 12-2 lb. bags per case distributed across multiple states and in Canada and Mexico. Consumers should not consume the product and are urged to seek refunds or replacements.
India's Fine Foods recalled 10 pieces of cookware on October 28, 2025, due to potential lead contamination. Consumers should not use the product and seek refunds or replacements. The recall affects cookware distributed in California and Washington.