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 deaths or serious injuries are reported, 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
About 133,000 Persilux zebra blinds are recalled because long operating cords pose strangulation and entanglement hazards to children, violating the federal window covering rule. No incidents reported.
Kia is recalling certain 2021-2023 Sorento vehicles because the heating, ventilation and air conditioning blower motor wiring harness may be inadequate, which can result in a fire.
Evenflo is recalling Gold Revolve360 Slim and Revolve360 Slim child seats because loose headrest foam can break off and pose a choking hazard to children.
3M Ranger Blood/Fluid Warming High Flow Sets are the subject of a field action to clarify flow rates, inlet fluid temperatures and the location of the outlet temperature. The FDA classified it as Class I.
Unichem Cyclobenzaprine Hydrochloride Tablets, 10 mg, lot GMML24026A, are recalled because bottles labeled as cyclobenzaprine contained yellow Meloxicam 7.5 mg tablets. The FDA classified the action as Class I.
Vegetable Tray Cucumbers in 3/2 lb cardboard boxes are recalled because the product is contaminated with Salmonella. The FDA classified the action as Class I.
Sliced Cucumber, 8 oz, sold in cardboard boxes, is recalled because the product is contaminated with Salmonella. The FDA classified the action as Class I. 89 boxes are affected.
Cucumbers Peeled/Diced 1/4 inch KBS in 5 lb cardboard boxes are recalled because the product is contaminated with Salmonella. The FDA classified the action as Class I.
Spanish Club Ciabatta, 10.5 oz, from Fresh and Ready Foods is recalled for undeclared wheat and milk. The FDA classified the action as Class I. 233 units are affected.
SmartDrive MX2+ SpeedControl Dials are recalled because a faulty electrical connection between the dial and the wheelchair motor may cause loss of control. The FDA classified the action as Class I. 25,389 units are affected.
Endico brand Peas & Carrots, 2.5 lb frozen bags produced 06/11/2025, are recalled because the product may be contaminated with Listeria monocytogenes. The FDA classified the action as Class I.
Piccolo Pranzo Box, 14.5 oz, from Fresh and Ready Foods is recalled for undeclared wheat and milk. The FDA classified the action as Class I. 233 units are affected.
SmartDrive MX2+ SpeedControl Dials, REF MX2-3DCMC, are recalled because a faulty electrical connection between the dial and the wheelchair motor may cause loss of control. 8,413 units are affected.
Chili Crunch Market Mezze, 14.5 oz, from Fresh and Ready Foods is recalled for undeclared wheat. The FDA classified the action as Class I. 233 units are affected.
Cucumber Sliced PLD KBS in 2/10 lb cardboard boxes, code X3234937, is recalled because the product is contaminated with Salmonella. The FDA classified the action as Class I.
Cucumber Peeled Sliced KBS in 2/5 lb cardboard boxes, code X3235434, is recalled because the product is contaminated with Salmonella. The FDA classified the action as Class I.
Endico brand Mixed Vegetables, 2.5 lb frozen bags produced 06/17/2025, are recalled because the product may be contaminated with Listeria monocytogenes. The FDA classified the action as Class I.
Honey Balsamic dressing in 3.4 ounce plastic pouches is recalled because it contains undeclared soy and sesame. The FDA classified the action as Class I. 46,800 units are affected.
Neuhaus Original Belgian Chocolate popping milk chocolates with cookies, 4.23 oz, are recalled because the product contains undeclared wheat. The FDA classified the action as Class I.
Tuscan Artichoke and Mozzarella Salad, 8.5 oz, from Fresh and Ready Foods is recalled for undeclared wheat and milk. The FDA classified the action as Class I. 233 units are affected.
SmartDrive MX2+ SpeedControl Dials, REF MX2-3DCK, are recalled because a faulty electrical connection between the dial and the wheelchair motor may cause loss of control. 15,834 units are affected.
Volkswagen is recalling one Audi SQ7 vehicle because the fasteners securing the high pressure fuel pump may not be tightened properly, resulting in a fuel leak. The vehicle has been repaired.
Volkswagen is recalling certain 2025-2026 GTI, Golf R, Audi A5, S5, A6 and Q4 e-Tron models because the torsion bar in one or both front seat belt retractors may have been damaged during production.
FLEX Monoclonal Mouse Anti-Human CD20cy for Dako Omnis, catalog GA60461-2J, is recalled because of the potential for weak staining that may result in false negative CD20 identification. 67 units are affected.
FLEX Monoclonal Mouse Anti-Human CD20cy for Dako Omnis is recalled because of the potential for weak staining, which may result in false negative CD20 identification. 4,145 units are affected.