Hazard
1,324 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 1,324 microbial contamination recalls we have scored against our rubric, 313 (24%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 678 (51%) 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 microbial contamination 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.
Medaus, Inc. is recalling Magnesium Chloride 200 mg/mL PF, 100 mL vials due to laboratory results indicating microbial contamination and concerns about the reliability of sterility testing.
JCB Labs LLC is recalling 903 vials of Acetylcysteine 20% Solution because laboratory results indicate microbial contamination and the sterility of the product cannot be assured.
Medaus, Inc. is recalling specific lots of Lipo-Injection w/ Lidocaine because laboratory results indicate microbial contamination and sterility cannot be assured.
Medaus, Inc. is recalling L-Glutathione 200 mg/mL PF, 100 mL, due to laboratory results indicating microbial contamination and concerns about the reliability of sterility testing.
Wellness Pharmacy is recalling Methyl B12 1 mg/mL single-use vials because laboratory results indicated microbial contamination and the FDA questioned the reliability of the testing.
Wellness Pharmacy is recalling 590 vials of Magnesium Sulfate Hepta 50% PF due to laboratory results indicating microbial contamination and concerns about the reliability of testing.
Wellness Pharmacy is recalling Phenylbutyrate 200 mg/mL vials because laboratory results indicate microbial contamination and the FDA has concerns about the reliability of the testing data.
Wellness Pharmacy is recalling 1,355 vials of Dexpanthenol 250 mg/mL due to laboratory results indicating microbial contamination and concerns about the reliability of testing.
Wellness Pharmacy is recalling Dexpanthenol 250mg/ml PF due to laboratory results indicating microbial contamination. The FDA expressed concern that the firm's contract testing lab results may not be reliable.
Wellness Pharmacy is recalling RL Glutathione 100 mg/mL vials due to laboratory results indicating microbial contamination and concerns about the reliability of testing.
Dr. Reddy's is recalling specific lots of OTC Ranitidine Hydrochloride tablets because raw material tested positive for Pseudomonas sp.
Vi-Jon, Inc. is recalling 18,408 bottles of Alcohol Free Antiseptic Mouth Rinse because a stability sample was found to be contaminated with Burkholderia contaminans.
Tarmac Products, Inc. is recalling specific lots of Well at Walgreens Regular Strength Antacid Liquid due to elevated microbial counts and E. Coli contamination.
Dr. Reddy's is recalling specific lots of Amoxicillin for Oral Suspension because testing revealed yeast and mold growth.
Chu Minh Corp is recalling fresh and fried tofu products because they were produced in a facility without available hot water.
Humco Holding Group is recalling Mercuroclear Antiseptic Anesthetic First Aid products due to potential contamination with Burkholderia gladioli. The recall covers 1,269,846 bottles distributed nationwide.
Lee Pharmaceuticals is recalling 12-Hour Sinus Nasal Spray products due to microbial contamination identified during testing.
Remel Inc is recalling 10 units of a lyophilized growth supplement for Legionella testing due to potential low-level microbial contamination.
Matrixx Initiatives Inc is recalling Zicam Extreme Congestion Relief nasal spray due to potential contamination with Burkholderia cepacia. The recall covers 46,752 bottles distributed nationwide.
American Enterprises LLC is recalling 750 kgs of Limed Bone Gelatin due to possible C. difficile contamination in the raw material.
DermaCare is recalling 43,272 bottles of UP & UP brand kids' foaming hand sanitizer due to high microbial counts.
DermaCare is recalling UP & UP brand kids' foaming hand sanitizer sold at Target due to laboratory findings of high total plate count above specification.
Raritan Pharmaceuticals is recalling Premier Value Fiber Plus Calcium Supplement Capsules due to possible C. difficile contamination in raw materials.
Raritan Pharmaceuticals is recalling Leader Fiber Capsules due to possible C. difficile contamination found in raw materials.
Raritan Pharmaceuticals is recalling Wal-Mucil Plus Calcium Fiber Capsules due to possible C. difficile contamination found in raw materials.