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
Linde Gas LLC is recalling 283 oxygen cylinders in Ohio because expired calibration equipment may have caused incorrect filling levels.
Hospira, Inc. is recalling 164,568 containers of Magnesium Sulfate in Water for Injection because the product contained higher levels of magnesium sulfate than specified.
Teva Pharmaceuticals is recalling 40,750 dispensers of Jolessa contraceptive tablets because some packages may be missing placebo tablets.
Bausch & Lomb is recalling 59,777 bottles of Murocel Lubricant Ophthalmic Solution because the product failed antimicrobial effectiveness testing.
Meridian Medical Technologies is recalling 83,400 Diazepam autoinjectors because they contain high levels of carbostyril, a known degradation product.
Airgas Inc is recalling 123 cylinders of Carbon Dioxide, USP, Medical Gas due to out-of-specification levels of nitrogen dioxide. The affected product was distributed to medical facilities in Arizona and California.
Hospira, Inc. is recalling specific lots of Propofol Injectable Emulsion because a single visible particulate was observed in a retention sample.
Luitpold Pharmaceuticals is recalling concentrated sodium chloride injection vials because visual particles were found in retention samples.
Noven Pharmaceuticals is recalling 244,320 Daytrana patches because the delivery system is miscalibrated or defective, making it difficult to remove the release liner.
Noven Pharmaceuticals is recalling Daytrana transdermal patches because the release liner may be difficult to remove. This could affect the patient's ability to apply the medication correctly.
Ben Venue Laboratories is recalling Octreotide Acetate Injection vials because some may have low fill volume. The recall covers 6,515 packs distributed nationwide and in Puerto Rico.
Physicians Total Care is recalling specific lots of Arthrotec 75 tablets because they may contain broken tablets. The recall affects products distributed in North Carolina and Kentucky.
Ben Venue Laboratories is recalling Midazolam HCl Injection vials because some may have low fill volume. The recall covers 11,161 packs distributed nationwide and in Puerto Rico.
Endo Pharmaceuticals is recalling specific bottles of Endocet 10 mg/650 mg tablets because some contained mixed 10 mg/325 mg tablets.
Noven Pharmaceuticals is recalling 335,190 Daytrana patches because the delivery system may be miscalibrated or defective, affecting the ability to remove the release liner.
Noven Pharmaceuticals is recalling 357,510 Daytrana (methylphenidate) patches because the delivery system may be miscalibrated or defective, affecting the ability to remove the release liner.
Quadrant Chemical Corporation is recalling DermaZinc Spray because the product is subpotent and does not meet the labeled 0.25% zinc pyrithione level.
Rugby Children's Pain & Fever Concentrated Drops are recalled because the dispensing dropper lacks child-resistant packaging, posing a risk of accidental overdose.
Procter & Gamble is recalling Vicks Dayquil Cold & Flu Liquicaps because the packaging failed to meet child-resistant closure requirements.
Lex Pharmaceutical is recalling approximately 25,000 bottles of vitamins and medicines because they lack required child-resistant packaging, posing a poisoning risk to children.
PL Development is recalling 3,798 bottles of CVS Sleep Caplets because they lack required child-resistant packaging, posing a poisoning risk to children.
Revco is recalling approximately 7,000 bottles of Revco Brand Pain Reliever because they were not packaged in child-resistant containers as required by law.
Moore Medical is recalling 11,000 bottles of Valumed Diphenhydramine Hydrochloride capsules because they lack required child-resistant closures, posing a poisoning risk to children.
Armour Pharmaceutical is replacing child-resistant caps on thyroid tablets because some adults could not properly close them, posing a poisoning risk to children.
Bristol Myers is substituting Excedrin analgesic tablets because packages failed to meet federal child-resistant regulations. The recall covers 225 and 375 tablet sizes distributed nationwide prior to April 1977.