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
Ace Surgical Supply Co. is recalling 25 vials of Succinylcholine 20 mg/mL due to an incorrect expiration date on the outer poly bag labeling.
Dr. Reddy's is recalling Doan's Pain Relieving Cream because the lot number on the outer packaging does not match the bottle. This is a Class III labeling recall.
SCA Pharmaceuticals is recalling specific lots of fentanyl and ropivacaine CADD cassettes due to a lack of assurance of sterility.
SCA Pharmaceuticals is recalling 487 syringes of Rocuronium Bromide 10 mg/mL due to a lack of assurance of sterility. The product was distributed nationwide.
SCA Pharmaceuticals is recalling 1,248 syringes of Succinylcholine 20 mg/mL due to a lack of assurance of sterility. The product was distributed nationwide.
SCA Pharmaceuticals is recalling 128 syringes of Hydromorphone HCL 1 mg/mL due to a lack of assurance of sterility. The product was distributed nationwide.
SCA Pharmaceuticals is recalling specific lots of morphine sulfate injection due to a lack of assurance of sterility.
SCA Pharmaceuticals is recalling 60 bags of Hydromorphone and Bupivacaine injection due to a lack of assurance of sterility.
SCA Pharmaceuticals is recalling 116 bags of fentanyl and bupivacaine injection due to a lack of assurance of sterility.
Kiriko, LLC. is recalling A1 Slim dietary supplements because FDA analysis found undeclared sibutramine, phenolphthalein, and n-desmethyl sibutramine.
SCA Pharmaceuticals is recalling 450 bags of oxyTOCIN 30 units in Lactated Ringers due to a lack of assurance of sterility.
SCA Pharmaceuticals is recalling 76 bags of Calcium Gluconate 2 g in 0.9% Sodium Chloride due to a lack of assurance of sterility.
SCA Pharmaceuticals is recalling 1,221 syringes of Phenylephrine HCl 100 mcg/mL due to a lack of assurance of sterility.
Teva Pharmaceuticals is recalling specific lots of Dutasteride and Tamsulosin HCl capsules because they failed dissolution specifications.
AvKARE is recalling 274 cartons of Duloxetine Delayed-release Capsules 20 mg due to slightly elevated levels of phthalic acid.
Precision Dose Inc. is recalling Carbamazepine Oral Suspension USP unit dose cups because they tested below the required potency specifications.
Sanofi-Aventis is recalling 422 vials of Clofarabine injection because the authorized generic product was packaged with the incorrect package insert for the brand name product.
Lucky Mart Inc. is recalling Piyamping Anti-Itch Lotion because it contains dexamethasone instead of the labeled hydrocortisone.
Vitility is recalling MAN OF STEEL capsules because FDA analysis found they contain undeclared sildenafil, an unapproved drug with unestablished safety and efficacy.
Pharmedium Services is recalling 6,108 bags of compounded Oxytocin 30 units in Lactated Ringer's because the drug was subpotent. The recall is voluntary and nationwide.
Baxter Healthcare is recalling 910 bags of Intralipid 20% because a portion of the lot was exposed to subfreezing temperatures during transit.
Banner Pharmacy Services is recalling 3,136 bags of Vancomycin 1.5 grams in 0.9% Sodium Chloride due to a lack of assurance of sterility.
Banner Pharmacy Services is recalling 1,359 bags of Diltiazem HCL 125 mg in 0.9% Sodium Chloride due to a lack of assurance of sterility.
Banner Pharmacy Services is recalling 966 cassettes of Midazolam HCL 100 mg due to a lack of assurance of sterility. The affected products were distributed nationwide.
Pharmedium Services is voluntarily recalling 42 bags of compounded Oxytocin 40 units in Lactated Ringer's solution because the drug was subpotent.