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
Zions RX Formulations is recalling 450 vials of Calcium Gluconate 10% for Injection due to a report of microbial contamination.
The FDA is recalling Vicerex male sexual enhancer capsules because laboratory analysis found undeclared tadalafil, an unapproved drug ingredient.
Slim Beauty USA is recalling Magic Slim capsules nationwide because they contain undeclared sibutramine and phenolphthalein, making them unapproved new drugs.
Terra-Medica Inc. is recalling Pleo Fort Suppositories because of penicillin cross-contamination. The product was distributed in the US, Canada, and the Philippines.
Zions RX Formulations Services LLC is recalling specific lots of Vitamin B-12 injections due to a lack of assurance of sterility resulting from poor aseptic practices.
Terra-Medica Inc. is recalling Pleo Quent Suppositories 3X due to penicillin cross-contamination. The product was distributed in the US, Canada, and the Philippines.
Terra-Medica Inc. is recalling Pleo Fort Tablets 5X due to penicillin cross-contamination. The product was distributed nationwide and internationally.
The FDA is recalling Black Ant dietary supplements because laboratory analysis found they contain undeclared sildenafil, an FDA-approved drug for erectile dysfunction.
Terra-Medica Inc. is recalling specific batches of Pleo Not DROPS homeopathic medicine due to penicillin cross contamination. The product was distributed in the US, Canada, and the Philippines.
Terra-Medica Inc. is recalling Pleo Ex DROPS 5X homeopathic antifungal medicine due to penicillin cross-contamination. The product was distributed in the US, Canada, the Philippines, and online.
Terra-Medica Inc. is recalling specific batches of Pleo Not Portable Sips oral homeopathic medicine because of penicillin cross-contamination.
Terra-Medica Inc. is recalling Pleo Not Portable Sips oral homeopathic medicine due to penicillin cross-contamination. The products were distributed in the US, Canada, and the Philippines.
Glenmark Generics Inc. is recalling specific bottles of Ranitidine Tablets USP 150 mg because they were found to contain foreign Metoprolol Tartrate tablets.
Terra-Medica Inc. is recalling Pleo Quent homeopathic medicine because of penicillin cross-contamination. The product was distributed in the US, Canada, and the Philippines.
Terra-Medica Inc. is recalling Pleo Nota-Quent Drops because of penicillin cross-contamination. The product is distributed in the US, Canada, and the Philippines.
Terra-Medica Inc. is recalling Pleo Quent capsules due to penicillin cross-contamination. The product was distributed in the US, Canada, and the Philippines.
Zions RX Formulations is recalling 861 bags of Magnesium Sulfate in Lactated Ringers due to poor aseptic practices that compromise sterility assurance.
Terra-Medica Inc. is recalling specific batches of Pleo Stolo DROPS 6X homeopathic medicine due to penicillin cross-contamination. Consumers should stop using the product and contact the company for a refund.
Terra-Medica Inc. is recalling Pleo Fort Portable Sips homeopathic medicine because of penicillin cross-contamination. The products were distributed in the US, Canada, and the Philippines.
Zions RX Formulations is recalling 610 units of Sodium Bicarbonate 8.4% injectable products due to a lack of assurance of sterility.
Zions RX Formulations is recalling 95 vials of Potassium Phosphates due to a lack of assurance of sterility caused by poor aseptic practices.
Terra-Medica Inc. is recalling Pleo Not Tablets 5X because of penicillin cross contamination. The affected homeopathic medicine was distributed in the US, Canada, and the Philippines.
Terra-Medica Inc. is recalling Pleo Not Suppositories 3X due to penicillin cross-contamination. The affected homeopathic medicine was distributed in the US, Canada, and the Philippines.
Terra-Medica Inc. is recalling specific batches of Pleo Quent DROPS 5X oral homeopathic medicine due to penicillin cross contamination.
Terra-Medica Inc. is recalling Pleo-Fort DROPS 5X homeopathic medicine due to penicillin cross-contamination. The product was distributed in the US, Canada, and the Philippines.