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.
Infiniti Creations, LLC is voluntarily recalling SkinEHCG HCG Drops due to misbranding and potential undeclared HCG content.
Infiniti Creations, LLC is voluntarily recalling HCG Complex drops due to misbranding and potential undeclared HCG content.
Infiniti Creations, LLC is voluntarily recalling Slim Life HCG Drops due to misbranding and potential undeclared HCG content.
Infiniti Creations, LLC is voluntarily recalling Simeons Program HCG Drops due to misbranding and potential undeclared HCG content.
DePuy Spine is recalling SKYLINE Variable Self-Tapping Screws because the packaging may contain Constrained Ti screws instead.
Infiniti Creations is voluntarily recalling Believe HCG Drops due to misbranding and potential undeclared HCG content.
Infiniti Creations, LLC is voluntarily recalling Omni Drops HCG products due to misbranding and potential undeclared HCG content.
DePuy Spine is recalling 14 units of SKYLINE Variable Self-Drilling Screws because they may have been packaged with Constrained Ti screws.
DePuy Spine is recalling 12 SKYLINE Anterior Cervical Plate System screws because they may have been packaged with the wrong screw type.
Infiniti Creations, LLC is voluntarily recalling A New You HCG Drops due to misbranding and potential undeclared HCG content.
DePuy Spine is recalling 9 units of SKYLINE Variable Self-Drilling Screws because they may have been packaged with Constrained Ti screws.
Infiniti Creations, LLC is voluntarily recalling Pounds and Inches 1oz HCG Drops due to misbranding and potential undeclared HCG content.
DePuy Spine is recalling 21 units of SKYLINE Anterior Cervical Plate System Constrained Self-Tapping Screws because Variable Ti screws may have been incorrectly packaged with them.
Infiniti Creations, LLC is voluntarily recalling Supervision Weightloss HCG Drops due to misbranding and potential undeclared HCG content.
Sandoz Inc is recalling 139,430 vials of Ceftriaxone Sodium for Injection in Wisconsin due to missing labels.
West-Ward Pharmaceuticals is recalling 32,102 bottles of Amoxicillin oral suspension because some bottles are missing the color-coded panel that displays the product strength.
Batista Bakery & Pastries, Inc. is recalling 30 units of Torpedo Rolls because the labels failed to declare wheat flour as required by FALCPA.
Batista Bakery & Pastries is recalling Portuguese Sliced Bread because the label failed to declare wheat flour as required by FALCPA.
Siemens is recalling Advia Chemistry Calibrators because incorrect values may cause a 41% positive bias in Direct Bilirubin patient results.
McCain Foods USA is recalling frozen onion rings sold under six private label brands because the product label does not declare milk.
Baptista Bakery & Pastries, Inc. is recalling Bulkie Rolls because the labels failed to declare wheat flour as required by FALCPA.
Batista Bakery & Pastries, Inc. is recalling 30 units of 16 oz. Italian Bread because the label fails to declare wheat flour as required by FALCPA.
C.R. Bard is recalling 75,089 Bard Inlay Ureteral Stents to add a warning about potential knots during removal.
Atrium Medical is recalling 20 Fr Trocar catheters because the packaging labels show more holes than the product actually contains.
C.R. Bard is recalling 75,089 Bard Inlay Optima ureteral stents to add a warning about potential knots during removal.