Hazard
9,607 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 9,607 mis labeling recalls we have scored against our rubric, 160 (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.
Cook Inc. is recalling 12,462 Amplatz Ultra Stiff Wire Guides because the label fails to state that the product is heparin-coated.
Cook Inc. is recalling 21,913 Movable Core Wire Guides because the labels failed to state that the products are heparin-coated.
Cook Inc. is recalling 10,367 Double Flexible Tipped Wire Guides because the labels fail to state that the product is heparin-coated.
Fresenius Medical Care is recalling NaturaLyte Liquid Acid Concentrate because some units in the affected lot had a potassium concentration of 2.25 mEq/L instead of the labeled 2.0 mEq/L.
Cook Inc. is recalling Newton Wire Guides because the labels do not state that the product is heparin-coated.
Cook Inc. is recalling 55 Reuter Tip Deflecting Wire Guides because the labels fail to state that the product is heparin-coated.
Arrow International is recalling 23,904 central venous catheter kits because some may be missing stickers with lot, expiration, and UDI information.
Cook Inc. is recalling 56 Left Atrial Catheter Sets because the labels failed to state that the product is heparin-coated.
Zimmer Biomet is recalling 24 units of Trabecular Metal Primary Hip Prostheses due to mislabeling. The affected devices were distributed in the US and several international countries.
Becton Dickinson & Co. is recalling 216 bottles of Difco Agar Noble because the product was mislabeled and inadvertently sold as Noble Agar.
Randox is recalling 450 kits of Liquid Cardiac Control CQ5053 because the product does not meet its shelf-life claim, potentially causing test results to fall outside control ranges.
Arrow International is recalling 23,904 central venous catheter kits because some units may be missing stickers with lot, expiration, and UDI information.
3M is recalling Futuro and ACE ankle supports because they contain natural latex rubber but lack the required caution statement.
Cook Inc. is recalling the Bentson Plus Wire Guide because the label fails to state that the product is heparin-coated.
Cook Inc. is recalling Bentson Wire Guides because the labels fail to state that the product is heparin-coated.
Zimmer Biomet is recalling 23 units of 36mm Modular Hip Heads because one piece was incorrectly etched with the wrong offset size.
Cook Inc. is recalling 32,340 Amplatz Stiff Wire Guides because the labels fail to state that the product is heparin-coated.
Cook Inc. is recalling 266 femoral artery pressure monitoring sets because the labels fail to state that the product is heparin-coated.
Cook Inc. is recalling 3,369 Coons Interventional Wire Guides because the label fails to state that the product is heparin-coated.
Cook Inc. is recalling 2,210 Fixed Core Bentson devices because the labels fail to state that the product is heparin-coated.
Cook Inc. is recalling 3,364 units of TFE Coated Curved Newton LLT because the label fails to state that the product is heparin-coated.
Cook Inc. is recalling Rosen Curved Wire Guides because the labels fail to state that the product is heparin-coated.
Zimmer Biomet is recalling six 6.5mm x 125mm x 16mm Cannulated Screws because they were mislabeled as 3.5mm x 24mm Cortical Locking screws.
Cook Inc. is recalling 601,778 Fixed Core Wire Guides because the labels failed to state that the products are heparin-coated.
Arrow International is recalling 23,904 central venous catheter kits because some may be missing stickers with lot numbers, expiration dates, and UDI information.