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
Sun Pharmaceutical Industries is recalling CEQUA (cyclosporine) ophthalmic solution due to subpotent drug levels and the presence of particulates.
KVK-Tech, Inc. is recalling 17,096 bottles of Hydrocodone Bitartrate and Homatropine Methylibromide tablets due to failed impurities and degradation specifications.
Fresenius Medical Care is recalling 709 cases of Delflex Peritoneal Dialysis Solution because a 4.25% dextrose bag was found inside a 1.5% dextrose box.
Nomax Inc. is voluntarily recalling 78 cartons of Dry Eye Test strips due to subpotent drug content. The FDA classified this as a Class III recall.
SigmaPharm Laboratories LLC is recalling Asenapine Sublingual Tablets because they were manufactured with the incorrect flavoring agent.
SigmaPharm Laboratories is recalling Asenapine sublingual tablets because they were manufactured with the wrong flavoring agent.
CareFusion 213, LLC is recalling Chloraprep One-Step applicators because the endcap may fall off during activation, releasing glass shards into the solution.
Sun Pharmaceutical Industries is recalling 50,868 bottles of Metformin Hydrochloride Extended-Release Tablets because activated carbon was found in the product.
QMart is recalling Burro en Primavera capsules because FDA analysis found unapproved tadalafil and/or sildenafil.
Antoto-K is recalling Thumbs Up 7 Red 70K because FDA analysis found unapproved sildenafil and tadalafil. The product was marketed without an approved NDA or ANDA.
QMart is recalling PremierZen Extreme 3000 capsules because FDA analysis found unapproved drugs tadalafil and/or sildenafil.
QMart is recalling Imperial Gold 2000 male sexual performance enhancement capsules because FDA analysis found undeclared tadalafil and/or sildenafil.
QMart is recalling Imperial Platinum 2000 capsules because FDA analysis found unapproved ingredients tadalafil and/or sildenafil.
PNHC, LLC. is recalling 139,806 bottles of Heal The World hand sanitizer because the packaging resembles drinking water bottles.
A-S Medication Solutions is recalling Health Essentials Kits containing Acetaminophen 500mg tablets. The bottles were incorrectly labeled with prescription drug labels instead of OTC labels.
Heritage Pharmaceuticals is recalling 408 bottles of Acyclovir 400 mg tablets distributed in Ohio due to incorrect or missing lot and expiration dates.
CareFusion 213, LLC is recalling ChloraPrep One-Step applicators because fungal growth breached package integrity. The product is a sterile skin antiseptic.
CareFusion 213, LLC is recalling Chloraprep One-Step antiseptic applicators because fungal growth breached package integrity. The product is distributed nationwide and internationally.
CareFusion is recalling ChloraPrep antiseptic applicators because fungal growth breached package integrity. The product is non-sterile, but the breach compromises the sterility of the applicators.
Na Na Collection is recalling Triple SupremeZen Gold 3500 capsules because FDA analysis found unapproved active ingredients tadalafil and/or sildenafil.
Preferred Pharmaceuticals is recalling six bottles of Cephalexin for Oral Suspension because an unidentified impurity was detected during testing.
Namoo Enterprise LLC is recalling PremierZen Black 5000 capsules because FDA analysis found unapproved ingredients tadalafil and sildenafil.
CareFusion 213, LLC is recalling ChloraPrep One-Step applicators due to a lack of assurance of sterility. The product may allow fungal growth at labeled storage conditions, potentially breaching package integrity.
S & B Story LLC is recalling Imperial Extreme 2000 Capsules because FDA analysis found unapproved ingredients tadalafil and sildenafil.
PD-Rx Pharmaceuticals is recalling Losartan Potassium 50 mg tablets because they contain trace amounts of NMBA, a potential carcinogen.