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
Handicare AB is recalling nine Carina mobile lifts because they were delivered with locking pins that are too small. This defect may cause increased wear on internal components.
Abbott is recalling 1,385 ARCHITECT c4000 cuvette segments because a detached post may cause falsely depressed patient results in adjacent cuvettes.
Firefly Medical is recalling 570 IVEA units because dowel pins can rotate and dislodge from leg castings after repeated use.
Permobil is recalling 146 electric wheelchair bases due to a potential failure of the top plate assembly that connects the seating system to the base.
Permobil is recalling 5,539 Corpus II electric wheelchairs because the top plate assembly may fail, potentially disconnecting the seating system from the base.
Radiometer America is recalling AutoCheck5+ Level 2 quality control ampoules because they may provide incorrect pCO2 and pO2 results.
The Metrix Company is recalling Secure 100mL empty vinyl containers because the hot stamp label incorrectly states the material. The bags are correctly made of PVC.
Bomimed is recalling specific lots of Disposable Fiber Optic Medium Laryngoscope Handles due to a potential for intermittent lighting during use.
Implant Direct is recalling 50 units of Swish Duo-Grip Healing Collars because the packages contained the wrong component size.
Carl Zeiss Meditec AG is recalling nine INTRABEAM PRS 500 radiation therapy devices because they had incorrect printed calibration values on their certificates.
The Binding Site Group is recalling 361 Human Alpha-1-Antitrypsin Kits because the high control may recover low and fall out of range.
Zimmer Biomet is recalling 4,423 ECT Internal Fracture Fixation Drills because raw material anomalies may increase the risk of instrument fracture during use.
Zimmer Biomet is recalling 1,129 orthopedic surgical drills and screw taps due to raw material anomalies that may increase the risk of instrument fracture.
Zimmer Biomet is recalling specific orthopedic drill bits and screw taps because raw material anomalies may cause the instruments to fracture during use.
Zimmer Biomet is recalling specific orthopedic surgical instruments due to a raw material anomaly that may increase the risk of instrument fracture during use.
Zimmer Biomet is recalling specific orthopedic drill bits and screw taps because raw material anomalies may increase the risk of instrument fracture during use.
Spectranetics is recalling Bridge Occlusion Balloon catheters because the guidewire may not pass through the device, potentially delaying treatment.
Zimmer Biomet is recalling 62 units of 4.0 mm Straight Shank Drill Bits because raw material anomalies may increase the risk of instrument fracture during use.
Zimmer Biomet is recalling 150 nonsterile orthopedic drill bits because raw material anomalies may cause the instruments to fracture during use.
Zimmer Biomet is recalling 15 nonsterile orthopedic drill bits because raw material anomalies may increase the risk of instrument fracture during use.
Sorin Group is recalling 72 Platinium VR implantable cardioverter defibrillators due to a possibility of overconsumption following electrostatic discharge or MRI scans.
Zimmer Biomet is recalling ECT Internal Fixation Drill Bits because raw material anomalies may cause the instruments to fracture during use.
Zimmer Biomet is recalling 182 M/DN Intramedullary Fixation Distal Drill Pilot Tips due to raw material anomalies that may increase the risk of instrument fracture.
Sorin Group is recalling Platinium VR implantable cardioverter defibrillators due to a possibility of overconsumption following electrostatic discharge or MRI scans.
Zimmer Biomet is recalling 62 ECT Internal Fracture Fixation Quick-Connect Drills because raw material anomalies may cause the instruments to fracture during use.