Browse through 2,313 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Ascend Laboratories recalled atorvastatin calcium tablets on September 19, 2025, due to failed dissolution specifications. The recall affects 90-count, 500-count, and 1000-count bottles. Consumers should stop using these medications immediately.
Black Sheep Egg Company recalled 23,400 dozen eggs on September 19, 2025, due to potential Salmonella contamination. The eggs were distributed in Arkansas and Missouri, with additional locations in Mississippi, Texas, California, and Indiana. Consumers should not consume the affected products and seek refunds or replacements.
Ascend Laboratories recalled 141,984 bottles of Atorvastatin Calcium Tablets on September 19, 2025. The recall follows a failure to meet dissolution specifications. Consumers should stop using the product immediately and consult healthcare providers.
Black Sheep Egg Company recalled 14,220 dozen eggs on September 19, 2025 due to potential Salmonella contamination. The recall affects Medium Brown Eggs sold in Arkansas and Missouri, with distribution in several other states. Consumers should not consume the eggs and are urged to seek refunds.
Black Sheep Egg Company recalled 46,800 dozen eggs on September 19, 2025, due to potential Salmonella contamination. The recall affects loose open skid eggs sold in retail and wholesale locations across Arkansas and Missouri, as well as broker locations in Mississippi, Texas, California, and Indiana. Consumers should not consume the affected eggs and seek refunds or replacements.
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.
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.
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.
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.
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.
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.
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.
Cook Medical recalled 695 Zenith Alpha 2 Thoracic Endovascular Grafts on September 18, 2025. The recall follows reports that PTFE coating scrapings could cause intravascular embolization during deployment. Patients and healthcare providers must stop using the device immediately.
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.