Hazard
2,547 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 2,547 infection recalls we have scored against our rubric, 31 (1%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,678 (66%) 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 infection 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.
Main Street Family Pharmacy is recalling compounded methylprednisolone vials after seven reports of skin abscesses.
Main Street Family Pharmacy, LLC is recalling preservative-free methylprednisolone 80mg/ml vials after seven reports of skin abscesses.
Main Street Family Pharmacy, LLC is recalling HCG 200 iu prefilled syringes due to adverse reactions reported for a different compounded product.
Main Street Family Pharmacy is recalling 196 units of B-12 mixture after seven reports of skin abscesses linked to a related compounded product.
Main Street Family Pharmacy is recalling 2 units of compounded methylprednisolone vials due to reports of skin abscesses.
Main Street Family Pharmacy is recalling 26 units of Mitomycin/Mannitol after seven reports of skin abscesses linked to a related compounded product.
Main Street Compounding Pharmacy is recalling compounded preservative-free methylprednisolone vials due to reports of skin abscesses.
Main Street Compounding Pharmacy is recalling Testosterone Cypionate vials due to adverse reactions reported with a different compounded product.
Main Street Family Pharmacy is recalling 62 vials of Testosterone Cypionate/Propionate after receiving seven reports of skin abscesses.
Main Street Family Pharmacy is recalling compounded Testosterone 200mg 30ml vials after receiving reports of skin abscesses linked to a related compounded product.
Main Street Family Pharmacy, LLC is recalling Betamethasone 6mg 10ml vials after receiving seven reports of skin abscesses potentially linked to the product.
Main Street Family Pharmacy is recalling 39 units of Adenosine 35 mg/ml after receiving seven reports of skin abscesses.
Main Street Family Pharmacy is recalling four units of Methylcobalamin 1000mcg/ml 30ml vials due to adverse reaction reports linked to a related compounded product.
Main Street Family Pharmacy, LLC is recalling Methylcobalamin 1mg/ml 50ml vials due to adverse reactions reported for a different compounded product.
ConMed is recalling 147 Altrus Thermal Tissue Fusion handpieces because they were exposed to higher-than-acceptable particulate matter during manufacture.
ConMed is recalling 65 Altrus Thermal Tissue Fusion handpieces exposed to excessive particulate matter during manufacture, which could cause minor local infections.
Fresenius Medical Care is recalling Liberty Cyclers because fluid leaks may contaminate dialysate, potentially causing peritonitis.
Medaus, Inc. is recalling Testosterone Cyp 200 mg/mL injections because laboratory results indicate microbial contamination and the sterility of the product cannot be assured.
Beacon Hill Medical Pharmacy is recalling Glycyrrhizic Acid 8 mg/mL Injectable because FDA inspectional findings raised concerns about sterility assurance.
Beacon Hill Medical Pharmacy is recalling Potassium Chloride 2 mEq/mL Injectable because FDA inspectional findings raised concerns about sterility assurance and quality control procedures.
Beacon Hill Medical Pharmacy is recalling Dextrose PF 50% Injectable because FDA inspections raised concerns about quality control and sterility assurance.
The FDA is recalling Naltrexone 1 mg/mL and 200 mg/mL injectables compounded by Beacon Hill Medical Pharmacy due to quality control issues affecting sterility assurance.
Beacon Hill Medical Pharmacy is recalling EDETATE DISODIUM 150 MG/ML INJECTABLE because FDA inspectional findings raised concerns about quality control procedures impacting sterility assurance.
Beacon Hill Medical Pharmacy is recalling L-Tryptophan 300 mg/mL injectable due to FDA inspectional findings regarding sterility assurance.
Pharmacy Creations is recalling EDTA disodium 150 mg/mL sterile injection vials due to a lack of assurance of sterility.