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
Herbal Doctor Remedies is recalling Lung Saver Capsules because they were manufactured outside of current Good Manufacturing Practices controls.
AAA Pharmaceutical is recalling Smart Sense Regular Strength Aspirin Tablets due to an incorrect expiration date on the label.
Wise Pharmacy is recalling Acetylcysteine 2% Otic Drops due to a lack of processing controls. The product was distributed in Colorado, Texas, and Wyoming.
ImprimisRx NJ is recalling 246 bottles of Timolol-Dorzolamide-Latanoprost ophthalmic drops because the medication was found to be subpotent.
Jubilant Cadista Pharmaceuticals is recalling specific lots of Drospirenone and Ethinyl Estradiol Tablets because they failed dissolution specifications during stability testing.
LNK International is recalling specific lots of Equate Nighttime Sleep Aid because of microbial contamination in the non-sterile product.
Wise Pharmacy is recalling 14 vials of compounded Papaverine/Phentolamine/Alprostadil/Atropine injectable due to a lack of processing controls.
ImprimisRx NJ is voluntarily recalling 405 bottles of Timolol-Latanoprost P-F ophthalmic drops because the medication was found to be subpotent.
NingBo Huize Commodity Co., Ltd. is recalling Tootsie Roll POP Orange Scented Antibacterial Hand Gel because stability testing was not conducted.
Wise Pharmacy is recalling 8 vials of Papaverine/Phentolamine Injectable due to lack of processing controls. The product was distributed in Colorado, Texas, and Wyoming.
NingBo Huize Commodity Co., Ltd. is recalling ICEE Peach Scented Antibacterial Hand Gel because stability testing was not conducted on the product.
Major Pharmaceuticals is recalling 828 cartons of Divalproex Sodium Extended-Release Tablets because they were exposed to high humidity during packaging.
NingBo Huize Commodity Co., Ltd. is recalling 20,160 units of Pink Lemonade Scented Antibacterial Hand Gel because stability testing was not conducted.
Wise Pharmacy is recalling 27 vials of Dexamethasone Sodium Phosphate Injection because of a lack of processing controls. The product was distributed in Colorado, Texas, and Wyoming.
Wise Pharmacy is recalling Gentamicin Irrigation Solution due to a lack of processing controls. The affected product was distributed in Colorado, Texas, and Wyoming.
Wise Pharmacy is recalling specific lots of compounded Papaverine/Phentolamine/Alprostadil injectable vials due to a lack of processing controls.
Wise Pharmacy is recalling Tobramycin Irrigation 80 mg/1000 mL Solution due to a lack of processing controls. The product was distributed in Colorado, Texas, and Wyoming.
Wise Pharmacy is recalling 32 vials of compounded Papaverine/Phentolamine/Alprostadil injectable due to a lack of processing controls. The product was distributed in Colorado, Texas, and Wyoming.
Lupin Pharmaceuticals is recalling Kaitlib Fe chewable tablets because long-term stability testing showed out-of-specification impurities or degradation.
Wise Pharmacy is recalling 84 vials of compounded Papaverine/Phentolamine/Alprostadil injectable due to a lack of processing controls.
Wise Pharmacy is recalling Alprostadil 100 mcg/mL Injectable vials due to a lack of processing controls. The product was distributed in Colorado, Texas, and Wyoming.
American Health Packaging is recalling Doxycycline Hyclate 100 mg tablets because they failed to meet dissolution specifications. The affected lot was distributed nationwide.
Piramal Critical Care is recalling Gablofen (baclofen injection) due to the presence of an unknown impurity observed during shelf life.
Pharma Pac is recalling specific lots of Neomycin Ophthalmic Ointment due to insufficient quality assurance controls in the manufacturing facility.
Wise Pharmacy is recalling 97 vials of compounded Papaverine/Phentolamine/Alprostadil injectable due to a lack of processing controls.