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
Oklahoma Respiratory Care Inc. is recalling 94 cylinders of compressed oxygen in Oklahoma because purity readings were out of specification.
West-Ward Pharmaceutical Corp. is recalling specific lots of Belladonna Alkaloids with Phenobarbital Tablets due to the presence of black specks comprised of degraded organic material.
Vi-Jon, Inc. is recalling 18,408 bottles of Alcohol Free Antiseptic Mouth Rinse because a stability sample was found to be contaminated with Burkholderia contaminans.
Max Huber Research Labs is recalling LA MER SPF 18 Fluid Tint because the active ingredient avobenzone may be subpotent, potentially reducing the product's sun protection.
Watson Laboratories is recalling Diclofenac Sodium and Misoprostol tablets because some are broken. Patients should stop using the product and contact their healthcare provider.
Max Huber Research Labs is recalling LA MER SPF 18 Fluid Tint because the active ingredient avobenzone may be subpotent, potentially reducing the product's effectiveness.
Pharmalucence, Inc. is recalling Technetium Tc 99m Sestamibi Injection kits due to the presence of particulate matter found in retained samples.
Max Huber Research Labs is recalling LA MER SPF 18 Fluid Tint because the active ingredient Avobenzone may be subpotent, reducing sunscreen effectiveness.
Watson Laboratories is recalling two lots of Oxycodone and Acetaminophen Capsules because the oxycodone content was found to be below specification at expiry.
Church & Dwight is recalling Arm & Hammer Sodium Bicarbonate Powder due to the presence of stainless steel and other foreign substances.
Fresenius Kabi is recalling 221,600 vials of Oxytocin Injection, USP, due to a subpotent drug issue identified during a 15-month stability test.
Apotex Corp. is recalling 37,303 vials of Piperacillin and Tazobactam for Injection due to a risk of precipitation or crystallization in IV bags or lines.
Sandoz Incorporated is recalling Estarylla tablets because a placebo tablet was found in a row of active tablets, which could reduce contraceptive effectiveness.
Church & Dwight is recalling Arm & Hammer Sodium Bicarbonate Powder due to the presence of stainless steel and other foreign substances.
Church & Dwight is recalling Arm & Hammer Sodium Bicarbonate Powder due to the presence of stainless steel and other foreign substances.
Church & Dwight is recalling Arm & Hammer Sodium Bicarbonate Powder due to the presence of stainless steel and other foreign substances.
American Health Packaging is recalling Quetiapine Fumarate 25mg tablets because they failed a dissolution test during stability studies.
Teva Pharmaceuticals is recalling specific lots of Amoxicillin for Oral Suspension because of orange to brown discoloration found on the inner foil seal.
Bayer HealthCare Pharmaceuticals Inc. is recalling 194.62 kg of Medroxyprogesterone acetate API because it failed stability specifications for particle size.
Olympia Pharmacy is recalling Betamethasone Sodium Phosphate 12 mg/ml Injection because FDA inspections raised concerns about quality control and sterility assurance.
Olympia Pharmacy is recalling Oxytocin 20 units/ml Injection because FDA inspections raised concerns about quality control and sterility assurance.
Olympia Pharmacy is recalling Metoclopramide 5 mg/ml Injection because FDA inspections raised concerns about quality control and sterility assurance.
Olympia Pharmacy is recalling Detomidine w/Xylazine Injection due to FDA inspection findings regarding quality control and lack of assurance of sterility.
Olympia Pharmacy is recalling compounded HCG injections because FDA inspections raised concerns about quality control and sterility assurance.
Olympia Pharmacy is recalling Dexamethasone Sodium Phosphate 6 mg/ml Injection because FDA inspections raised concerns about quality control and sterility assurance.