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
Emerson is recalling specific Fisher pressure relief valves used in cargo tank trailers because they may break and eject, posing risks of injury, fire, or road hazards.
Delicious Beef Jerky, LLC is recalling 8 pounds of Lemon Pepper Seasoned Beef Jerky because the products were produced and shipped without the required USDA inspection.
Ford is recalling 2013-2014 C-Max, Fusion, Escape, and Lincoln MKZ vehicles because a defect in the Restraint Control Module may prevent airbags and seat belt pretensioners from functioning in a crash.
Polaris is recalling 2015 Victory motorcycles because a transmission spring may be installed incorrectly, potentially causing loss of control.
Mercedes-Benz is recalling 2015 C300 and C400 vehicles because a steering component may disengage, potentially causing loss of control.
Foster Farms is recalling approximately 39,747 pounds of frozen chicken breast strips due to possible Listeria monocytogenes contamination. The product was distributed to California, Texas, Utah, and Washington.
Caviness Beef Packers is recalling approximately 23,100 pounds of beef trimmings produced in August 2014 due to possible E. coli O157:H7 contamination.
Nova Products, Inc. is voluntarily recalling Black Ant capsules because FDA analysis found undeclared sildenafil, an active ingredient in erectile dysfunction drugs.
Dean Foods is recalling Swiss Premium 100% Pure Orange Juice from Concentrate in half-gallon and one-gallon plastic containers due to undeclared dairy ingredients.
Nova Products, Inc. is voluntarily recalling XZEN GOLD capsules because FDA testing found undeclared sildenafil and tadalafil.
Dean Foods is recalling Lehigh Valley Dairy Farms Orange Juice from concentrate because it contains undeclared dairy. The product was distributed in several Mid-Atlantic states.
Vibrant Health is recalling Rainbow Vibrance Hi ORAC Superfood because a raw material used in its manufacture was found to contain Salmonella bacteria.
Nature's Universe is recalling ThinoGenics dietary supplements because they contain undeclared sibutramine and were marketed without FDA approval.
Dean Foods is recalling Lehigh Valley Dairy Farms Orange Juice from Concentrate because it contains undeclared dairy. The product was distributed in several Mid-Atlantic states and Washington, DC.
Nova Products, Inc. is voluntarily recalling Xzen 1200 capsules because FDA analysis found undeclared sildenafil and tadalafil, active ingredients in erectile dysfunction drugs.
Nova Products, Inc. is voluntarily recalling African Black Ant capsules because FDA testing found undeclared sildenafil, an active ingredient in erectile dysfunction drugs.
Nova Products, Inc. is voluntarily recalling XZEN Platinum capsules because FDA analysis found undeclared sildenafil and tadalafil.
Vibrant Health is recalling Green Vibrance 15 dietary supplements because a raw material used in manufacturing was found to contain Salmonella bacteria.
Baxter Healthcare is recalling specific lots of 0.9% Sodium Chloride Injection USP bags due to the presence of particulate matter, including fibers and plastics.
American Health Packaging is recalling 137,300 Ibuprofen 600 mg tablets because some cartons were mis-labeled as Oxcarbazepine 300 mg.
Brooks Tropicals, LLC is recalling avocados found positive for Salmonella. The affected product was distributed in Florida, Georgia, Illinois, New Jersey, and New York.
Bristol-Myers Squibb is recalling Coumadin for Injection vials because metallic-like and cellulose fiber particles were found in retained samples.
Baxter Healthcare is recalling 390,560 bags of 0.9% Sodium Chloride Injection USP due to the presence of particulate matter, including fibers and plastics.
Swanson Health Products is recalling 544 containers of 1 lb Certified Organic Carob Powder due to a potential risk of Salmonella contamination from a raw ingredient.
Nova Products, Inc. is voluntarily recalling Mojo Risen because FDA testing found undeclared sildenafil, an active ingredient in erectile dysfunction drugs.