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.
S & B Story LLC is recalling Imperial Extreme 2000 Capsules because FDA analysis found unapproved ingredients tadalafil and sildenafil.
Na Na Collection is recalling Triple SupremeZen Gold 3500 capsules because FDA analysis found unapproved active ingredients tadalafil and/or 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 HCG 340 iu prefilled syringes due to adverse reactions reported for a different compounded product.
Main Street Family Pharmacy, LLC is recalling 543 units of Estradiol Pellets 6mg after receiving reports of skin abscesses.
Main Street Compounding Pharmacy is recalling Carnitine 250mg/ml vials due to reports of skin abscesses linked to a different compounded product.
Main Street Compounding Pharmacy is recalling HCG 180 iu prefilled syringes after receiving reports of skin abscesses linked to compounded methylprednisolone.
Main Street Family Pharmacy is recalling 8 units of Lipotropic 30ml vials after receiving seven reports of skin abscesses potentially linked to the product.
Main Street Compounding Pharmacy is recalling 744 units of Amikacin 500mg 2ml following reports of adverse reactions.
Main Street Compounding Pharmacy is recalling Sodium Tetradecyl Sulfate 3.0% vials due to reports of skin abscesses linked to a different compounded product.
Main Street Family Pharmacy, LLC is recalling HCG 100 iu prefilled syringes due to reports of adverse reactions involving skin abscesses.
Main Street Family Pharmacy is recalling 151 units of compounded Testosterone 210mg 10ml vials due to adverse reactions reported for a related product.
Main Street Compounding Pharmacy is recalling Double Strength PGE1 40mcg 2ml vials due to reports of skin abscesses linked to a related compounded product.
Main Street Compounding Pharmacy is recalling 59 units of Lipotonix Plus w/Proc/Chrom after receiving seven reports of skin abscesses potentially linked to the product.
Main Street Family Pharmacy, LLC is recalling AMIC-12 with lido 10ml vials due to reports of skin abscesses.
Main Street Family Pharmacy, LLC is recalling Alprostadil 20mcg/ml 25ml vials after receiving seven reports of skin abscesses.
Main Street Compounding Pharmacy is recalling Special Mic Formula 30ml vials after receiving seven reports of skin abscesses potentially linked to the product.
Main Street Family Pharmacy is recalling Carnitine 250mg/ml after receiving seven reports of skin abscesses potentially linked to the product.
Main Street Family Pharmacy is recalling 1,250 units of Testosterone Pellets 200mg after receiving seven reports of skin abscesses.