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
The C F Sauer Company is recalling Monarch Breakfast Syrup in 1.5 oz cups due to undeclared peanuts. The product was distributed in Florida, Maryland, South Carolina, and Tennessee.
SS Wholesale Inc. is recalling eXtenZone capsules because FDA analysis found undeclared desmethyl carbondenafil and dapoxetine, making the product an unapproved new drug.
FDA is recalling Rhino 5 capsules marketed as a dietary supplement because they contain undeclared desmethyl carbondenafil and dapoxetine, making them unapproved new drugs.
IQ Formulations is recalling Hydravax High Potency Diuretic Weight Loss Solution because it contains an undeclared prescription diuretic, Triamterene.
NuVision Pharmacy is recalling 122 vials of Sermorelin/GHRP-6 due to lack of sterility assurance identified during an FDA inspection.
SS Wholesale Inc. is recalling MaXtremeZEN capsules because FDA analysis found undeclared desmethyl carbondenafil and dapoxetine, making the product an unapproved new drug.
L. M. Noodle Company, LLC is recalling Marlyce's Homemade Butterballs because the label fails to declare wheat, soy, whey, and milk.
Health Wright Products Inc is recalling Digestive Enzyme Supplements contaminated with Chloramphenicol. The products were distributed to California, Florida, Oregon, Utah, and Mexico.
Health Wright Products Inc is recalling Zinc Plus dietary supplements because they were made from an ingredient contaminated with Chloramphenicol.
DeRoyal Industries is recalling 2 units of the Aquarius Hot/Cold Therapy Combo Unit due to temperature monitoring failures and electric shock reports.
Health Wright Products Inc. is recalling Enzyme Formula dietary supplements because they were made from ingredients contaminated with Chloramphenicol.
The Mentholatum Company is recalling several Rohto eye drop products due to concerns about the quality assurance of sterility controls.
Health Wright Products Inc. is recalling B-Complex with Enzymes supplements contaminated with Chloramphenicol. The affected product was distributed to five US states and Mexico.
DeRoyal Industries is recalling 738 Aquarius Temperature Therapy units because they fail to monitor water temperature, posing a risk of temperature injuries and electric shock.
Codman & Shurtleff is recalling 895 Certas Programmable Valves used for hydrocephalus because they may not operate properly.
DeRoyal Industries is recalling 409 Aquarius Hot/Cold Therapy Combo Units because they fail to monitor water temperature, posing a risk of temperature injuries and electric shock.
Health Wright Products Inc is recalling B-Complex Plus dietary supplements because they were made from an ingredient contaminated with Chloramphenicol.
DeRoyal Industries is recalling 25 Aquarius Hot/Cold Therapy Combo Units because they fail to monitor water temperature, posing a risk of temperature injuries and electric shock.
NuVision Pharmacy is recalling 285 vials of HCG (Lyophilized) nationwide due to a lack of sterility assurance identified during an FDA inspection.
The Mentholatum Company is recalling several Rohto eye drop products due to concerns about the quality assurance of sterility controls.
The Mentholatum Company is recalling Rohto eye drops because of concerns about sterility controls. The recall covers nationwide distribution and Puerto Rico.
The Mentholatum Company is recalling several Rohto eye drop products due to concerns about the quality assurance of sterility controls.
DeRoyal Industries is recalling 48 Aquarius Hot/Cold Therapy Combo Units because they fail to monitor water temperature and have caused electric shocks.
The Mentholatum Company is recalling Rohto eye drops because of concerns about the quality assurance of sterility controls.
Codman & Shurtleff is recalling 369 Certas Programmable Valves used for hydrocephalus because they may not operate properly.