Hazard
9,610 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 9,610 mis labeling recalls we have scored against our rubric, 161 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 588 (6%) 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 mis labeling 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.
Teleflex Medical is recalling 6,390 sterile tracheal tubes because some units labeled as 7mm may actually be 7.5mm.
Greiner Bio-One is recalling 4 ml FX Sodium Fluoride/Potassium Oxalate tubes because they may contain low or no additives, potentially affecting glucose and lactate test results.
Synthes (USA) Products LLC is recalling 14 units of 1.5 mm Rapid Resorbable Orbital Floor Plates because outer package expiration dates may exceed subcomponent dates.
Synthes (USA) Products LLC is recalling 22 units of 1.5 mm Rapid Resorbable Orbital Floor Plates because outer package expiration dates may exceed subcomponent dates.
Ellipse A/S is recalling 14 Ellipse ND: YAG Laser applicators because they lack required instructions for calibration procedures and schedules.
Synthes (USA) Products LLC is recalling Norian Drillable Inject 10 CC-Sterile units because the internal rotary pouch may be labeled with the incorrect powder volume, though the actual contents are correct.
Medical Components, Inc dba MedComp is recalling specific lots of Tearaway Introducers because they are labeled with incorrect expiration dates.
East Manufacturing is recalling 2016 Hybrid and Steel Dump trailers with overstated weight ratings that could lead to overloading and crashes.
Gulf Stream is recalling 2016-2017 Ameri-Lite and Super-Lite trailers because the Federal Certification label lists incorrect tire and wheel sizes, which could lead to installing the wrong replacement parts.
1888653 Ontario Inc. is recalling specific EVOS Full Face Modular Helmets that may not adequately protect the wearer's head in a crash and lack required safety labeling.
Southeast Toyota Distributors is recalling 2015-2016 Toyota and Scion vehicles because the load carrying capacity label may be incorrect, potentially leading to vehicle overload.
World's Choice Products is recalling 610 bottles of New Life Nature's Blend 100% Multivitamin Juice because the product contains undeclared whey protein and soy lecithin.
Pronutri, LLC is recalling 356 bottles of Re-VITA-lize Tropical Orange Dietary Supplement due to undeclared milk and soy lecithin.
Giant Eagle is recalling Walnut Delights 6 Packs because the labels fail to declare the milk ingredient and allergen.
World's Choice Products is recalling Xtreme Fiber Detox because it contains undeclared whey protein (milk) and soy lecithin.
Ouhlala Gourmet is recalling raspberry fruit tartlets because the finished product labeling fails to declare milk as an ingredient.
Ouhlala Gourmet LLC is recalling lemon fruit tartlets because the finished product contains undeclared milk. The recall covers 9,159 cases distributed nationwide and internationally.
Giant Eagle is recalling Pecan Tassies because the ingredient and allergen statements fail to declare milk. This poses a risk to consumers with milk allergies.
Frank L Harter & Sons is recalling 5 lb containers of Spinach Dip because the label failed to list milk and soy as ingredients.
Frank L Harter & Sons Inc. is recalling 548 cases of 5 lb pasta salad containers because the labels failed to list milk and soy as ingredients.
Frank L Harter & Sons Inc. is recalling Hawaiian Delight salad due to missing milk and soy allergen labeling.
Ventlab LLC is recalling STAT-Check Resuscitation Bags because the carbon dioxide indicators are non-functional and fail to change color during use.
Giant Eagle is recalling Pecan Tassies because the packaging fails to declare milk as an ingredient or allergen.
Blue Bell Creameries is recalling 23,973 pints of Rocky Road ice cream sold in Texas and Louisiana because the product may contain undeclared wheat and soy.
MicroAire is recalling 20 Pneumatic Impactor units because they are missing required lock and unlock symbol markings.