Hazard
238 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 238 adverse reaction recalls we have scored against our rubric, 2 (1%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 233 (98%) 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 adverse reaction 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.
Flow Beverages Inc. is recalling Flow Alkaline Spring Water (Organic lemon & ginger, 500 ml) due to four customer complaints of alleged adverse reactions. Affected lots are 2023AUG29 V5, distributed to eleven states.
Flow Beverages Inc. is recalling Flow Alkaline Spring Water in organic lemon and ginger flavor due to four customer complaints of alleged adverse reactions. The affected product was distributed across multiple U.S. states.
QMart is recalling PremierZen Extreme 3000 capsules because FDA analysis found unapproved drugs tadalafil and/or sildenafil.
Na Na Collection is recalling Triple SupremeZen Gold 3500 capsules because FDA analysis found unapproved active ingredients tadalafil and/or sildenafil.
S & B Story LLC is recalling Imperial Extreme 2000 Capsules because FDA analysis found unapproved ingredients tadalafil and sildenafil.
Market America is recalling 1,496 bottles of bliss anti-stress formula dietary supplement due to potentially undeclared Yohimbe and reported adverse reactions.
Gadget Island, Inc. is recalling PapaZen 3300 capsules because they contain undeclared prescription drugs sildenafil, desmethyl carbodenafil, and tadalafil.
Organic Herbal Supply is recalling ZRECT Male Enhancement capsules because FDA analysis found undeclared prescription drugs, including tadalafil and sildenafil.
Health & Beyond is recalling Tranquility dietary supplements because they contain unapproved prescription drugs, Doxepin and Chlorpromazine.
Main Street Family Pharmacy, LLC is recalling 415 units of Brompheniramine 10ml due to seven reports of skin abscesses.
Main Street Family Pharmacy is recalling 894 units of Ascorbic Acid 500mg/ml 50ml vials due to adverse reaction reports linked to a related compounded product.
Main Street Family Pharmacy, LLC is recalling HCG 220 iu prefilled syringes due to reports of adverse reactions involving skin abscesses.
Main Street Family Pharmacy is recalling Lido 2% MPF 2ml vials due to reports of skin abscesses linked to the product.
Main Street Family Pharmacy, LLC is recalling Mic B-Complex 50ml vials after seven reports of skin abscesses potentially linked to the product.
Main Street Family Pharmacy is recalling compounded preservative-free methylprednisolone 80mg/ml 10 ml vials due to reports of skin abscesses.
Main Street Family Pharmacy, LLC is recalling 11 units of Minoxidil 10% 60ml. The recall follows seven reports of skin abscesses linked to a different compounded product.
Main Street Family Pharmacy is recalling 7 units of Tri-Mix SS Pap 30mg, Phen 1mg, PGE1 10mcg 10ml vials due to reports of skin abscesses.
Main Street Family Pharmacy is recalling HCG 15,000u vials due to reports of skin abscesses linked to compounded methylprednisolone.
Main Street Family Pharmacy is recalling 10 units of compounded methylprednisolone injections after receiving seven reports of skin abscesses.
Main Street Family Pharmacy is recalling Testosterone Pellet 87.5mg units due to seven reports of skin abscesses.
Main Street Compounding Pharmacy is recalling 43 units of Medroxyprogesterone (PF) 150mg/10ml after receiving seven reports of skin abscesses.
Main Street Compounding Pharmacy is recalling Lipotonix Plus-Mic B complex due to reports of skin abscesses linked to a related compounded product.
Main Street Family Pharmacy is recalling Single Strength PGE1 20mcg/ml vials after receiving seven reports of skin abscesses potentially linked to the product.
Main Street Family Pharmacy is recalling 14 units of compounded Testosterone Cypionate/Propionate 250mg 10ml vials due to adverse reaction reports.
Main Street Family Pharmacy is recalling Lipotropic 50ml vials due to seven reports of skin abscesses linked to a related compounded product.