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.
Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.
The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.
Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.
Minimum severity
Stryker Howmedica Osteonics Corp. is recalling T2 K-Wires because a packaging review found that the seal integrity of the pouch may be decreased.
Stryker Howmedica Osteonics Corp. is recalling T2 Guidewires because a packaging review found that the seal integrity of the pouch may be decreased.
Bigwall Enterprises is recalling WARM STEAM Personal Steam Inhalers nationwide due to unconfirmed consumer complaints. No causal link to product use has been established.
Stryker is recalling T2 K-Wires because the packaging seal integrity may be decreased, potentially affecting the sterility of the medical devices.
Zimmer Biomet is recalling 289 CPT 12/14 COCR hip prostheses because the LDPE packaging bag adheres to the implant surface.
Zimmer Biomet is recalling 194 Metasul Head 40 total hip prosthesis components because the packaging bag adheres to the implant surface.
Fresenius Medical Care is recalling Naturalyte Liquid Acid Concentrate because the label incorrectly lists the calcium concentration.
Zimmer Biomet is recalling 101 Versus 7.5 inch hip prostheses because the LDPE packaging bag adheres to the implant surface.
Olympus Scientific Solutions Americas is recalling Delta XRF Analyzers because the firm discovered a software bug.
Zimmer Biomet is recalling NexGen Knee CR femoral components because the packaging bag adheres to the implant surface.
Becton, Dickinson and Company is recalling 78 units of BD FMC7 FITC reagent because the vial labels display an incorrect expiration date.
Zimmer Biomet is recalling CR Flex and LPS Flex knee prostheses because the LDPE packaging bag adheres to the polished implant surface.
Medtronic is recalling 364,768 Endo GIA Ultra Universal Short Stapler Handles because they may fail to fire or partially fire, and the articulating lever may disengage during use.
Medtronic is recalling 2,711 Best Practice Kits containing specific Endo GIA Ultra Universal Stapler Handles due to reports of staplers failing to fire or partially firing, and articulating levers disengaging during use.
Medtronic is recalling 1,102,166 Endo GIA Ultra Universal Standard Stapler Handles worldwide because they may fail to fire or partially fire during surgery.
Varian Medical Systems is recalling Eclipse Treatment Planning System versions 11, 13.0, 13.5, and 13.6 due to a dose calculation error that may result in unintended radiation exposure.
Medtronic is recalling 327,797 Endo GIA Ultra Universal 12 mm XL Stapler Handles worldwide because the staplers may fail to fire or the articulating lever may disengage during surgery.
Smith & Nephew is recalling 203 High Flow Irrigation Extenders because the device body may separate during surgery, potentially obstructing visualization and causing fluid leakage.
Bio-Rad is recalling 278 EVOLIS Microplate Systems because a low fluid alarm could cause the plate transport to continue running, pushing plates off the transporter.
Philips is recalling actuator assemblies for angiographic x-ray monitor ceiling suspension systems because the actuator can detach, causing the monitor carriage to drop.
Nihon Kohden America Inc is recalling MEE-1000A Neuromaster accessories due to defective printed circuit boards that failed to prevent unintentional current flow.
ViewRay is recalling five MRIdian Radiation Therapy Systems because they loaded a completion fraction in the incorrect order after a treatment interruption.
CareFusion 303, Inc. is recalling 9,345 Jadak Barcode Scanners used with Pyxis Anesthesia systems because they may transmit incorrect medication information to the dispensing system.
Leica Microsystems is recalling Bond Polymer Refine Red Detection kits due to a manufacturing error that may cause inadequate staining.
Smith & Nephew is recalling 8 units of Legion Hemi Stepped Tibial Wedges because the included screws were too long to properly affix the device.