Hazard
60 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 60 incorrect dosage recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 39 (65%) are Severe.
Which agencies issued them
Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all incorrect dosage recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.
A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.
TG United, Inc. is recalling Poly-Vent IR and DM tablets because they are underdosed or have an incorrect dosage regime.
TG United, Inc. is recalling 886 bottles of AMBI 40PSE/400GFN tablets because the products are underdosed or have an incorrect dosage regime.
TG United, Inc. is recalling Mesehist DM cough and cold medicine because the product is underdosed or has an incorrect dosage regime.
TG United, Inc. is recalling BroveX PSB Liquid antihistamine and decongestant products because they are underdosed or have an incorrect dosage regime.
TG United, Inc. is recalling 13,031 bottles of TL-Hist PD Drops because the product is underdosed or has an incorrect dosage regime.
TG United, Inc. is recalling NoHist Tablets because they are underdosed or have an incorrect dosage regime.
TG United, Inc. is recalling CPM / PSE Drops because the products are underdosed or have an incorrect dosage regime.
TG United, Inc. is recalling BroveX PSB DM Liquid antihistamine and decongestant products because they are underdosed or have an incorrect dosage regime.
Abbott Laboratories is recalling specific lots of Synthroid (levothyroxine sodium) tablets because bottles labeled as 150 mcg actually contained 75 mcg tablets.
Varian Medical Systems is recalling ARIA Radiation Oncology Version 11 software because monitor units may be incorrect when continuing partial treatment.