Hazard
245 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 245 undeclared ingredient recalls we have scored against our rubric, 55 (22%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 41 (17%) 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 undeclared ingredient 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.
Fabscout Entertainment, Inc. is recalling Clalis capsules because FDA analysis found they contain sildenafil, an undeclared active pharmaceutical ingredient.
IQ Formulations is recalling Hydravax High Potency Diuretic Weight Loss Solution because it contains an undeclared prescription diuretic, Triamterene.
SS Wholesale Inc. is recalling MaXtremeZEN capsules because FDA analysis found undeclared desmethyl carbondenafil and dapoxetine, making the product an unapproved new drug.
Zi Xiu Tang Success, LLC is recalling Ultimate Formula capsules because they contain undeclared sibutramine, an ingredient removed from the market for safety reasons.
Zi Xiu Tang Success, LLC is recalling Classic Zi Xiu Tang Bee Pollen Capsules because they contain undeclared sibutramine, an unapproved active ingredient.
Beamonstar Products is recalling SexVoltz All Natural Herbal Supplement because it contains tadalafil, an unapproved drug ingredient.
Beamonstar Products is recalling Velextra All-Natural Herbal Supplement because it contains tadalafil, an unapproved drug ingredient.
Ann's House of Nuts is recalling Daily Chef Tropical Fruit & Nut Blend because it contains undeclared Yellow #5 and #6 dyes.
Chang Kwung Products is recalling Lightning ROD capsules because FDA analysis found an undeclared analogue of sildenafil, an unapproved new drug.
Chang Kwung Products is recalling Lightning ROD capsules because FDA analysis found an undeclared analogue of sildenafil, making the product an unapproved new drug.
NOW Foods is recalling Ashwagandha Extract capsules because they contain undeclared licorice extract. Consumers should stop using the product.
Arizona Beverages USA LLC is recalling 10,286 cases of 1-gallon Arizona Southern Style Unsweetened Brewed Tea due to an undeclared Splenda ingredient.
InSo-Independent Contractor for West Coast Nutritionals, LTD is recalling three unapproved male enhancement products found to contain undeclared tadalafil.
The Menz Club is recalling Blue Male Enhancement Pill because it contains sulfoaildenafil, an unapproved analogue of sildenafil.
Coral Rock Man, Inc. is recalling X-Rock 3 Day Pill For Men because the product was marketed without an approved NDA/ANDA and tested positive for Sildenafil and analogs.
SunFresh Natural LLC is recalling 1,200 bags of 6-ounce pitted prunes nationwide because the product contains unapproved Rhodamine B45170 and undeclared sorbic acid.
Pepsi Bottling Group Nashville is recalling 2-liter bottles of Diet Orange Crush because they contain undeclared high fructose corn syrup.
The Menz Club, LLC is recalling V Maxx Rx because FDA testing found it contains an unapproved drug analogue.
Spillson's, Ltd. is recalling Double Cheeseburger Sandwiches because they contain undeclared soy lecithin. The source text notes a risk of serious reaction for people with wheat allergies.
Namias dba Chonita Foods is recalling 22 cases of Sonoran Rice due to undeclared hydrolyzed soy protein. The product was distributed only in Arizona.