Browse through 642 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Zydus Pharmaceuticals recalled 912 bottles of Entecavir Tablets on September 24, 2025, due to failed impurity specifications. The recall affects 30-count bottles of 0.5 mg tablets Distributed nationwide in the USA.
Scott & Jon's Honey Sesame Salmon Rice Bowl is recalled due to undeclared wheat. The recall affects 966 cases distributed across multiple states. Consumers should stop using the product and contact the manufacturer for refunds.
El Rojo Wholesale recalled 2,904 units of Wheat Pellets on September 23, 2025. The product lacks an ingredient list and nutritional panel, posing a risk to consumers. The absence of wheat and Yellow No. 6 could cause serious health issues for those with allergies.
RC Outsourcing LLC recalled 2,669 syringes of Bevacizumab on September 22, 2025. The recall stems from a lack of assurance of sterility, raising significant health risks. Healthcare providers and consumers should stop using the product immediately.
Arizer recalled Solo II portable vaporizers on September 18, 2025, due to fire hazards. Affected devices can overheat and eject materials, posing burn risks. Consumers should stop using the product immediately and seek a replacement.
LXDHSTRA recalled baby loungers on September 18, 2025, due to suffocation and fall hazards. The loungers violate federal safety standards for infant sleep products. Consumers must stop using them immediately and return them for a full refund.
IcyBreeze recalled its Buddy portable misting fan on September 18, 2025, due to a fire hazard. The device can overheat while charging, posing a risk of ignition. Consumers should stop using the fan immediately and return it for a full refund.
Five Below recalled two models of tabletop fire pits due to burn hazards. The recall affects products sold from April 2024 through August 2025. Consumers reported risks of flash fires and flame jetting causing serious injuries.
Youbeien recalled crib mobiles on September 18, 2025, due to a risk of battery ingestion. The toys fail to meet safety standards and pose serious injury risks. Consumers should stop using the mobiles and contact GKKBSJ for refunds.
YooxArmor recalled multi-purpose kids' helmets on September 18, 2025. The helmets violate safety standards and pose a risk of serious head injuries. Consumers should stop using the helmets immediately and contact YooxArmor for a refund.
Wuensche USA recalled all Ambiano Cotton Candy makers on September 18, 2025. The heating element can ignite sugar, causing a fire hazard if used improperly. Consumers should stop using the product immediately and contact ALDI for a refund.
EnHomee recalled its Fabric 13-Drawer Dressers on September 18, 2025. The dressers pose a serious tip-over risk if not anchored to a wall. This recall affects an unspecified number of units sold by EnHomee Direct.
Egress Capital Partners recalled 3,547 cases of Taproom Gourmet bulk "Park" Mix on September 18, 2025. The product lacks an ingredient label and contains undeclared allergens including peanuts and almonds. Consumers should not consume the product and seek a refund.
B BRAUN MEDICAL recalled its PERIFIX FX Continuous Epidural Anesthesia Set on September 18, 2025. The recall affects a potential defect in the catheter connector lid position. This high-risk issue could impact patient safety in healthcare settings across the country.
B Braun Medical recalled the PERIFIX FX Continuous Epidural Anesthesia Tray on September 18, 2025. The manufacturer identified a potential issue with the catheter connector lid position. No injuries have been reported, but users should stop using the product immediately.
B Braun Medical recalled the PERIFIX FX Continuous Epidural Anesthesia Tray on September 18, 2025. The recall affects an unspecified number of units due to a potential connector misalignment. This issue poses a high risk to patient safety and requires immediate action from healthcare providers.
B Braun Medical recalled 2,760 units of its PERIFIX FX Continuous Epidural Anesthesia Tray on September 18, 2025. The recall stems from a potential misalignment of the catheter connector lid, posing a high risk to patients. Healthcare providers and patients must stop using the device immediately and follow the manufacturer’s instructions.
B Braun Medical recalled the PERIFIX FX Continuous Epidural Anesthesia Tray on September 18, 2025. The recall affects a potential safety issue with the catheter connector. No injuries have been reported but the hazard level is classified as high.
B Braun Medical recalled the PERIFIX FX Continuous Epidural Anesthesia Tray on September 18, 2025. The recall affects a potential defect in the catheter connector lid. Patients and healthcare providers must stop using the device immediately.
B Braun Medical recalled 2,840 anesthesia trays on September 18, 2025. The recall stems from a potential defect in the catheter connector lid position. The product poses a high hazard risk to patients and healthcare providers.