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
The FDA is recalling CaverFlo Natural Herbal Coffee because it contains undeclared sildenafil, tadalafil, and milk. The product was marketed without an approved NDA or ANDA.
C. O. Truxton is recalling specific lots of Phenobarbital Tablets USP, 30 mg, because they may be mislabeled. The FDA classifies this as a Class I recall.
The Harvard Drug Group is recalling Rugby Diocto Liquid due to microbial contamination, including yeast and potential B. cepacia.
The Harvard Drug Group is recalling Rugby Senexon Liquid due to microbial contamination, including yeast and potential B. cepacia.
The Harvard Drug Group is recalling Rugby Diocto Syrup due to microbial contamination, including yeast and potential B. cepacia.
The Harvard Drug Group is recalling Major Senna Syrup due to microbial contamination, including yeast and potential B. cepacia.
The Harvard Drug Group is recalling 4,715 bottles of Rugby Aller-chlor syrup due to microbial contamination, including yeast and potential B. cepacia.
PD-Rx Pharmaceuticals is recalling 3,440 bottles of Phentermine Hydrochloride capsules because stability tests showed out-of-specification unknown impurities.
C. O. Truxton is recalling Phenobarbital Tablets USP, 100 mg, due to a label mixup that may result in mislabeled products.
C. O. Truxton is recalling specific lots of Phenobarbital Tablets USP, 15 mg, due to a label mixup that may result in mislabeled products.
C. O. Truxton is recalling specific lots of Phenobarbital Tablets USP, 60 mg, due to a label mixup that may result in mislabeling.
C. O. Truxton is recalling specific lots of Amitriptyline HCL 50 mg tablets due to potential label mixups. The recall is nationwide.
Dynamic Technical Formulations is recalling Biotech Underground Tri-Ton Hardcore Formula capsules because FDA testing found unapproved drug ingredients.
Genetic Edge Compounds LLC is recalling GEC LX Laxoplex dietary supplements because FDA analysis found the product tainted with undeclared anabolic steroids and steroid-like substances.
Hardcore Formulations is recalling D-ZINE Rapid Size and Strength capsules because they contain unapproved active ingredients.
Hardcore Formulations is recalling Ultra-Sten capsules because they contain unapproved ingredients and were marketed without an approved NDA or ANDA.
ICU Medical Inc. is recalling 436,716 units of 0.9% Sodium Chloride Injection due to the presence of stainless steel particulate matter.
Global Marketing Enterprises is recalling 52.5 kg of unapproved caffeine powder marketed with stimulant claims and lacking adequate directions for use.
Lupin Limited is recalling Mibelas 24 Fe tablets because the first four pills in the packet are brown instead of the last four, and the expiry/lot was not printed on the package.
Amgen is recalling 175,632 vials of Procrit (Erythropoietin) because visible glass flakes were identified in some drug product vials.
AvKARE Inc. is recalling specific lots of Voriconazole Tablets, 200 mg, because they failed impurity specifications for a related compound.
Linde Eckstein is recalling specific lots of Make Up Perfect sand SPF 10 liquid make-up because the SPF 10 protection claim cannot be fully guaranteed.
Hetero USA Inc. is recalling 5,664 bottles of Entecavir 0.5 mg tablets because a single unknown impurity exceeded the allowed limit during stability testing.
Akorn Inc is recalling Chlorhexidine Gluconate Oral Rinse unit dose cups because crystallization caused subpotent assay results.
Linde Eckstein is recalling 373 bottles of SPF 10 liquid make-up because the sun protection claim cannot be guaranteed.