These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
2,251 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
B Braun Medical recalled 5,448 blood administration sets on October 29, 2025. The recall affects devices used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. The company cited potential backflow of medication and occlusion as the primary hazards.
B Braun Medical recalled 32,436 Anesthesia IV Sets on October 29, 2025. The recall affects specific catalog numbers due to a risk of medication backflow. Healthcare providers must stop using these devices immediately and follow the provided recall instructions.
B Braun Medical recalled 41,976 IV administration sets on October 29, 2025. The recall stems from a risk of medication backflow into primary IV containers. Affected products include catalog number 490354, distributed worldwide.
B Braun Medical recalled 31,392 IV administration sets on October 29, 2025, due to a high risk of medication backflow. The affected models include catalog number 490301. This recall affects devices distributed worldwide, including the US and Canada.
B Braun Medical recalled 41,016 IV administration sets on October 29, 2025. The recall addresses the risk of medication backflow into primary IV containers. This issue could lead to significant health risks for patients receiving intravenous therapy.
B Braun Medical recalled 4,536 IV administration sets on October 29, 2025. The recall affects devices that may allow backflow of medication from secondary IV containers. This poses a high risk to patients using the Infusomat Space, Outlook, and Vista Basic pumps.
B Braun Medical recalled 10,896 IV administration sets on October 29, 2025. The recall addresses a risk of medication backflow from secondary IV containers. This issue could lead to serious health risks for patients.
B Braun Medical recalled 1,861,111 IV administration sets on October 29, 2025. The recall addresses a significant risk of medication backflow from secondary IV containers into primary containers. Healthcare providers and patients must stop using the devices immediately.
B Braun Medical issued a recall for 1,250 IV administration sets on October 29, 2025. The recall stems from a potential backflow of medication between IV containers, posing a serious risk to patients. Healthcare providers and patients must stop using the devices immediately.
B Braun Medical recalled 1,080 IV administration sets on October 29, 2025. The recall affects sets used with the Infusomat Space, Outlook, and Vista Basic Pumps. The company identified a risk of backflow of medication from secondary IV containers into primary containers.
B Braun Medical recalled 29,900 IV Administration Sets on October 29, 2025. The recall follows reports of potential medication backflow and inability to prime. Healthcare providers and patients must stop using the device immediately.
B Braun Medical recalled 19,104 IV administration sets on October 29, 2025. The recall stems from a potential for medication backflow and inability to prime. The affected sets were distributed worldwide, including the US and Canada.
B Braun Medical recalled 27,480 IV extension sets on October 29, 2025. The recall affects devices tied to the Infusomat Space, Outlook, and Vista pumps. The company warns of potential medication backflow and occlusion issues that could endanger patients.
B Braun Medical recalled nearly 19,000 IV administration sets on October 29, 2025, due to a serious backflow risk. The affected products may allow medication to flow back from secondary containers into primary ones. This poses significant health risks to patients.
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.
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.
Moonlight Packing Corporation recalled 2,603 cases of sticker labels for Loose Bulk - peppermint peaches on October 28, 2025. The recall follows concerns of potential contamination with Listeria monocytogenes. Consumers should not consume these products and seek refunds or replacements.
Moonlight Packing Corporation recalled over 102,000 cases of yellow peaches on October 28, 2025. The recall follows potential contamination with Listeria monocytogenes. The affected peaches were distributed across multiple U.S. states and in Canada and Mexico.
Moonlight Packing Corporation recalled 2,375 cases of loose bulk white peaches on October 28, 2025. The recall stems from potential contamination with Listeria monocytogenes, a bacterium that can cause severe illness. Consumers should not consume the product and should seek a refund or replacement.
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.