Hazard
702 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 702 class i recalls we have scored against our rubric, 345 (49%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 343 (49%) 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 class i 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.
Chetak New York is recalling Deep-brand frozen garlic cloves after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen tindora after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen surti undhiu mix after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen mixed vegetables after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen suran after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen baby bhindi after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Africa Imports is recalling Organic Moringa Leaf Powder from lot SO-71449 after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Genepro Protein is recalling 250 bags of Genepro Whey 4th Generation protein because the labeling contains incorrect ingredient information and fails to declare milk as an allergen.
Alanwar Food Corp is recalling Sonex brand aluminum pots after the products were found to contain leachable lead levels of 0.323mg/L. The FDA has classified the action as Class I.
Fresenius Kabi USA is recalling 483 cases of Ivenix LVP Primary Administration Sets after incorrect assembly of a specific lot that the firm states could result in serious patient injury.
American Nuts is recalling 2,700 units of Dry Roasted Baking Macadamia Nuts over potential Salmonella contamination. The FDA has classified the action as Class I.
Glycar SA is recalling 30 SJM Pericardial Patches with EnCap Technology because the impacted lot may not meet the required tensile strength specification. The FDA classified it Class I.
WFM Purchasing is recalling 411 lbs of Whatcom Farmhouse sliced cheese sold at Whole Foods after WSDA testing identified potential STEC and E. coli O103 contamination.
Olympus is recalling 7,803 Single Use Ligating Devices because the ligation loop may fail to release or detach, leaving it unintentionally fixed around patient anatomy.
FRC Inc is recalling 16 units of Face Rock Creamery Vampire Slayer Garlic Cheddar after an FDA environmental sample found Listeria monocytogenes in the packaging area.
WFM Purchasing is recalling 411 lbs of Whatcom Blue sliced cheese sold at Whole Foods after WSDA testing identified potential STEC and E. coli O103 contamination. The FDA classified it Class I.
Fresenius Kabi is recalling 2,199,850 vials of Famotidine Injection USP after out of limit results were obtained for endotoxin testing. The FDA classified it Class I.
Glycar SA is recalling 18 SJM Pericardial Patches, 5 x 10 cm, because the impacted lot may not meet the required tensile strength specification. The FDA classified it Class I.
MeriCal is recalling 698,064 units of Member's Mark Super Greens Dietary Supplement over potential contamination with Salmonella Richmond. The FDA classified it Class I.
Twin Sisters Creamery is recalling 3,438.20 pounds of raw milk Whatcom Blue cheese due to E. coli O103:H2. The FDA has classified the recall as Class I.
Twin Sisters Creamery is recalling 1,359.86 pounds of raw milk Farmhouse Cheese due to E. coli O103:H2 and E. coli O74:H25. The FDA has classified the recall as Class I.
TMJ Solutions is recalling 63 TMJ Bilateral Implants because the patient-fitted temporomandibular joint implant contained a discrepancy in screw hole position. The FDA classified it Class I.
Publix Super Markets is recalling 1,452 units of Publix Rich & Creamy Vanilla Ice Cream over undeclared eggs. The FDA has classified the recall as Class I.
Otsuka ICU Medical is recalling one lot of Potassium Chloride Injection because the overwrap label may state 10 mEq when the product is 20 mEq. The FDA classified it Class I.
Otsuka ICU Medical is recalling 21,696 containers of Potassium Chloride Injection 20 mEq in 50 mL because the overwrap may state 10 mEq. The FDA classified it Class I.