Hazard
9,611 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 9,611 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 589 (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.
Aidapak Services, LLC is recalling 3 mg Melatonin tablets because they may be mislabeled as other medications like Docusate Sodium or Pioglitazone.
The Anspach Effort, Inc. is recalling all lots of MCA Cutting Burrs and Dissection Tools because the indications for use were broader than validated and directions were unclear.
Aidapak Services, LLC is recalling aMILoride HCl 5 mg tablets because they may be mislabeled as Propranolol HCl 10 mg or Famotidine 20 mg.
Aidapak Services, LLC is recalling Riluzole 50 mg tablets due to a labeling error where they may be mislabeled as Trazodone HCl 150 mg.
Aidapak Services, LLC is recalling Lactobacillus tablets due to a label mixup that may cause them to be mislabeled as other medications.
Aidapak Services is recalling carbamazepine ER tablets that may be mislabeled as acarbose due to a label mixup.
Aidapak Services is recalling RANOLAZINE ER 500 mg tablets because they may be mislabeled as other medications. The repacked drugs were distributed in four western states.
The Anspach Effort, Inc. is recalling MCA Cutting Burrs and Dissection Tools because the indications for use were broader than validated and directions for use were unclear.
Aidapak Services is recalling Cranberry Extract/Vitamin C capsules because they may be mislabeled as other medications. The products were distributed in four western states.
Aidapak Services is recalling Tizanidine HCl tablets because they may be mislabeled as other prescription drugs. The repacked drugs were distributed in four western states.
Aidapak Services, LLC is recalling Isometheptene Mucate capsules because they may be mislabeled as other medications. The error could lead to patients receiving the wrong drug.
The Anspach Effort, Inc. is recalling Micro Curved Attachment Cutting Burrs because the indications for use were broader than validated and directions were unclear.
Aidapak Services, LLC is recalling Chlorophyllin Copper Complex tablets that may be mislabeled as trazodone hydrochloride.
Aidapak Services, LLC is recalling Pramipexole Di-HCl tablets because they may be mislabeled as Multivitamin/Multimineral or Perphenazine.
The Anspach Effort, Inc. is recalling MCA Cutting Burrs and Dissection Tools because the indications for use were broader than the device's validation.
The Anspach Effort, Inc. is recalling all lots of MCA Cutting Burrs and Dissection Tools because the indications for use were broader than the device's validation.
Aidapak Services is recalling Ribavirin capsules that may be mislabeled as Modafinil or Desipramine. The error involves incorrect product identification on the packaging.
Aidapak Services, LLC is recalling Zinc Sulfate capsules that may be mislabeled as Phosphorus tablets. The error involves a label mixup on repacked products.
Aidapak Services, LLC is recalling Lactobacillus Acidophilus capsules due to a potential labeling mixup with other medications.
Zimmer, Inc. is recalling 1,534 units of Palacos R+G Radioplaque Bone Cement because the lot number on the patient label may not match the outer carton.
Aidapak Services is recalling Levothyroxine/Liothyronine tablets that may be mislabeled as Magnesium Gluconate Dihydrate.
Aidapak Services is recalling Omeprazole/Sodium Bicarbonate capsules because they may be mislabeled as Lactobacillus GG or Pyridoxine HCL.
Aidapak Services is recalling Cilostazol 100 mg tablets because they may be mislabeled as Dutasteride 0.5 mg capsules.
Aidapak Services is recalling Omeprazole/Sodium Bicarbonate capsules because they may be mislabeled as Benzocaine/Menthol lozenges. The FDA classifies this as a Class II recall.
Aidapak Services, LLC is recalling guaiFENesin ER tablets because they may be mislabeled as prenatal multivitamin or other medications.