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
Advanced Pharma Inc. is recalling RECK PeriCapsular injection because the product may contain synthetic or natural latex, which is not clearly labeled.
Advanced Pharma Inc. is recalling all Lidocaine products because they may contain latex but lack appropriate labeling.
Advanced Pharma Inc. is recalling Ofirmev (Acetaminophen) injection because the product may contain synthetic or natural latex, which is not currently classified in the labeling.
Advanced Pharma Inc. is recalling TPN products because they may contain latex but lack proper labeling.
Advanced Pharma Inc. is recalling all lots of Norepinephrine Bitartrate because the product may contain synthetic or natural latex, which is not currently disclosed on the label.
Advanced Pharma Inc. is recalling Ropivacaine HCl in 0.9% Sodium Chloride because the product may contain synthetic or natural latex, which is not currently classified in the labeling.
Advanced Pharma Inc. is recalling all lots of Nalbuphine because the product labeling fails to disclose that it may contain synthetic or natural latex.
Advanced Pharma Inc. is recalling all lots of Lorazepam HCl because the product may contain synthetic or natural latex, which is not currently labeled.
Advanced Pharma Inc. is recalling Fentanyl Citrate and Bupivacaine HCl products because labeling may not disclose the presence of synthetic or natural latex.
Advanced Pharma Inc. is recalling NICU Starter TPN products because they may contain synthetic or natural latex without proper labeling.
Advanced Pharma Inc. is recalling all lots of Vancomycin HCl because the product may contain latex but lacks appropriate labeling.
Advanced Pharma Inc. is recalling all lots of Fentanyl Citrate because the product labeling does not indicate that it may contain synthetic or natural latex.
Advanced Pharma Inc. is recalling all lots of Meperidine HCl because the product labeling does not indicate that it may contain synthetic or natural latex.
Advanced Pharma Inc. is recalling 0.9% Sodium Chloride Slip Tip products because they may contain latex without proper labeling.
Advanced Pharma Inc. is recalling all strengths and dosage forms of Heparin sodium because the product may contain synthetic or natural latex without proper labeling.
Advanced Pharma Inc. is recalling Sodium Phosphate products because they may contain latex but lack proper labeling. The recall covers all strengths and dosage forms distributed nationwide.
Advanced Pharma Inc. is recalling Calcium Gluconate products because they may contain latex without proper labeling.
Advanced Pharma Inc. is recalling all strengths and dosage forms of Sodium Citrate because the product may contain latex without proper labeling.
Advanced Pharma Inc. is recalling all strengths and dosage forms of Potassium Phosphate because the product may contain latex but lacks proper labeling.
Advanced Pharma Inc. is recalling Cardioplegic Solution Maintenance due to a labeling error regarding potential latex content.
Advanced Pharma Inc. is recalling all lots of Midazolam HCl because the product may contain synthetic or natural latex.
Advanced Pharma Inc. is recalling all lots of Ketamine HCl because the product may contain synthetic or natural latex.
Advanced Pharma Inc. is recalling all lots of Succinylcholine Chloride because the product may contain latex but lacks proper labeling.
Advanced Pharma Inc. is recalling all lots of Ephedrine Sulfate because the product may contain latex but lacks proper labeling.
Advanced Pharma Inc. is recalling all lots of Morphine Sulfate because the product labeling does not indicate that it may contain synthetic or natural latex.