Recalls
Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.
Minimum severity
General Motors is recalling certain 2025 and 2026 Chevrolet Corvettes with a software error that may prevent detection of rear turn signal failures. Drivers may be unaware the signal is not working, increasing crash risk.
Prima Vera Nueva, Inc. is recalling BBQ Chipotle Bean & White Cheddar Tamales in California and Nevada due to potential Listeria monocytogenes contamination.
BHARAT BAZAR is recalling SOMA KITCHEN NATURAL ASAFOETIDA due to undeclared wheat. The product may pose a health risk to consumers with wheat allergies.
Gold Star Distribution Inc is recalling toothbrushes due to potential exposure to rodents and rodent activity discovered at the manufacturer's distribution center. Products were distributed in Minnesota.
Cardinal Health chest drainage units are being recalled because the instructions needed clarification about intended use in adults aged 18+. When used on infants, the units may not show expected visual indicators, potentially leading to improper treatment assessment.
Medline recalled multiple medical procedure kits due to a defect causing butyrate tubing in MASTISOL liquid adhesive vials to crack during use. The affected kits are used in neurological and surgical procedures.
Medline Industries is recalling 1,928 units of two procedure convenience kits due to MASTISOL liquid adhesive vials with tubing that can crack during actuation, potentially affecting proper kit function.
Philips MR 7700 MRI systems with software versions R11.1 and R12.1 may display incorrect stiffness values from elastography maps in PACS viewers, potentially affecting diagnostic interpretation.
A Siemens LUMINOS interventional X-ray system may fail to flip ortho images as intended, risking processing of a previous patient's image. No illnesses or injuries have been reported.
Philips Ingenia 1.5T MRI systems with software versions R11.1 or R12.1 may display incorrect stiffness values when viewing MR Elastography images in medical imaging systems. Ten affected units have been identified worldwide.
The Alphenix INFX-8000C x-ray system's ceiling suspension screws may become loose, preventing lateral movement and causing sensor errors. 172 units distributed in the US and Dominican Republic are affected.
Ford is recalling certain 2022-2024 Maverick vehicles because the Body Control Module may deactivate one or both rear tail lights. This failure reduces vehicle visibility to other drivers, increasing crash risk.
Forest River and Coachmen are recalling 2024-2025 fifth wheel and travel trailers with removable step assemblies. Loose mounting bolts may allow the steps to detach during use, creating a risk of injury.
The FDA is recalling Genesis Screw-In Anchor devices due to reports of device failure including breakage, bending, and pull-out. Approximately 600 units distributed in California and Puerto Rico are affected.
Medline Industries recalls eight medical procedure kits nationwide due to MASTISOL liquid adhesive vials with cracking butyrate tubing. The defect could affect proper device function during cardiac and vascular procedures.
Medline is recalling multiple medical procedure convenience kits containing MASTISOL liquid adhesive because the butyrate tubing cracks during use, posing a potential safety risk. The recall affects 66 units distributed nationwide.
Medline medical procedure kits are being recalled due to complaints that butyrate tubing cracks during actuation of MASTISOL Liquid Adhesive vials. The kits are distributed nationwide.
NIPRO Technical Services is recalling Conductivity Standard Solutions due to defective conductivity values that cause meters to report incorrect readings for dialysate calibration.
Elekta is recalling approximately 5,391 medical linear accelerators (Synergy, Harmony, Infinity, Versa HD models) worldwide due to a manufacturing issue affecting electrical grounding systems.
Medline Industries is recalling 1,928 circumcision procedure kits due to cracked tubing in the included MASTISOL liquid adhesive. The defect occurred during actuation of the adhesive vials.
CareFusion is recalling 189 BD Alaris Pump Module model 8100 units with invalid daylight savings time timestamps that prevent connection to hospital networks, affecting device interoperability.
Mount Olive Pickle Company is recalling Hannaford brand hamburger dill pickle chips due to glass found in some jars. Consumers should not consume the affected product.
Winnebago is recalling approximately 1,166 motorhomes because the LED backlight circuit board in the cooktop range may overheat, increasing fire risk. Dealers will replace the cooktop control panel at no cost.
BMW is recalling certain 2017-2025 K 1600 motorcycles because the reverse gear control unit seal may deteriorate, allowing moisture inside and causing the unit to overheat. An overheated unit increases the risk of fire.
General Motors is recalling 2023–2025 Chevrolet Malibu vehicles with defective rearview cameras that may display distorted or blank images. This reduces visibility when backing, increasing crash risk.