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
Health Plus Incorporated is recalling Super Colon Cleanse capsules because the Drug Facts label incorrectly describes the active ingredient per dose instead of per capsule.
McNeil Consumer Healthcare is recalling Imodium Multi-Symptom Relief Caplets due to defective containers and damaged blister units.
Lloyd Inc is recalling 1,913,236 Thyro-Tab 0.75 mg tablets because they failed potency testing at the 6-month interval.
Physicians Total Care Inc. is recalling Methylprednisolone Tablets, USP, 4 mg, due to potential failure to meet Impurity C specifications.
Lloyd Inc is recalling 19,039 bottles of Levothroid 75 mcg tablets because the drug tested below the required potency level.
Lloyd Inc is recalling 19,166 bottles of Levothroid 50 mcg tablets because they failed potency testing at 9 months.
Lloyd Inc is recalling 1,924,297 bulk Thyro-Tab 0.050mg tablets because they failed potency testing at the 9-month interval. The product was distributed nationwide and to Puerto Rico.
Teva Pharmaceuticals is recalling specific lots of Zeosa chewable oral contraceptive tablets because they may not meet impurity specifications.
Teva Pharmaceuticals is recalling Mefloquine Hydrochloride 250 mg tablets because they may be underweight or overweight.
Shionogi Inc. is recalling Nisoldipine Extended Release Tablets, 17mg, because a specific lot failed USP dissolution testing requirements.
Physicians Total Care is recalling Morphine Sulfate tablets because bottles may be mislabeled, potentially containing the wrong formulation.
Physicians Total Care is recalling Morphine Sulfate Extended Release tablets because bottles may be mislabeled as Immediate Release or vice versa.
Abbott Laboratories is recalling Zemplar (paricalcitol) Injection due to a potential CGMP deviation where a foreign stopper may have been applied to vials.
Physicians Total Care is recalling specific lots of Lipitor (atorvastatin calcium) 40 mg tablets due to chemical contamination identified as 2,4,6 tribromoanisole.
Kutol Products Co Inc is recalling Hands Down Medicated Lotion Soap because it contains Red Dye #15, an ingredient not approved for use in drugs.
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.