Hazard
684 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all 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.
Medline Industries is recalling Pediatric Airway Procedure Kits containing Medline Neuro Sponges due to higher-than-expected endotoxin levels that may be out of specification.
Medline Industries is recalling medical procedure kits containing Medline Neuro Sponges due to higher-than-expected endotoxin levels that may be out-of-specification.
Medline is recalling medical procedure kits containing Neuro Sponges due to higher-than-expected endotoxin levels. The affected in-market product may be out-of-specification for endotoxin.
Milestone S.R.L. is recalling Vacuum Bag SU Large non-sterile specimen containers (Model 68409SS) due to the possibility of reagent leakage from the container. The recall affects approximately 61,600 units distributed worldwide.
LSL Healthcare is recalling its Standard Central Line Dressing Change Kit (Model 2717J) because the included Webcol Large Alcohol Prep Pads were found to be non-sterile.
Davol, Inc. is recalling Avitene Ultrafoam Microfibrillar Collagen Hemostat (Catalog Number 1050030) because the product may contain foreign matter, confirmed to be inspect fragments.
B. Braun Medical Inc. is recalling Lactated Ringers Irrigation 3000 mL bags due to lack of assurance of sterility and potential leakage from the diaphragm port after foil removal.
Fresenius Kabi USA is recalling batch 6402165 of 5% Dextrose Injection (NDC 65219-458-05/30) due to lack of assurance of sterility. The batch was distributed nationwide through May 30, 2028 and should not be used.
GoodSense Eye Drops Original Formula and related store brands are being recalled nationwide due to lack of assurance of sterility. The recall affects 378,144 bottles with specific lot numbers and expiration dates.
K.C. Pharmaceuticals recalls multiple brands of over-the-counter eye drops nationwide due to lack of assurance of sterility. Approximately 315,144 bottles are affected.
Tops GOLD Lime Pickle, a 31.74 oz product from Mangalm LLC, is recalled due to potential adulteration with erucic acid from mustard oil. The recall affects products distributed in CA, NV, OR, UT, and WA.
Beckman Coulter is recalling 685 boxes of MicroScan Neg MIC 56 diagnostic panels due to likely presence of contamination in test wells. The affected lot was distributed across 12 U.S. states.
Strides Pharma is recalling Children's Ibuprofen Oral Suspension due to the presence of gel-like masses and black particles found in the product. Affected lots 7261973A and 7261974A should not be used.
Wawa Beverage Company is recalling 5,456 units of Double Dutch Chocolate Milk (16 oz) because foreign plastic material was discovered on the fill line during production.
Wawa Beverage Company is recalling Wawa Cookies & Cream Milk (16 oz bottles) due to foreign plastic material discovered on the fill line.
Pitavastatin Calcium 2mg tablets distributed in Tennessee are being recalled after a 1mg tablet was found in a bottle. FDA classified this as Class III. No illnesses have been reported.
International Life Sciences recalls Artelon FlexBand Plus surgical devices (Ref 41054, 41057) worldwide due to bacterial endotoxin contamination discovered during testing.
Boston Scientific is recalling EndoVive Safety PEG Kits due to open or compromised seals on included ChloraPrep Triple Swabsticks that could result in loss of sterility or drying of antiseptic solution.
Radnostix recalls Sodium Iodide I-131 oral solution (FDA Class II) due to particulate matter contamination from production issues. Affected product was distributed nationwide in the USA and Puerto Rico.
Valley Springs bottled water products, including infant and pet water varieties, have been recalled due to being bottled under insanitary conditions. The recall affects approximately 379,868 units distributed in Illinois and Wisconsin.
LEO Pharma is recalling ADBRY (tralokinumab-ldrm) injectable medication due to wool fiber particles found in at least one unit, compromising sterility assurance of approximately 11,407 units distributed nationwide.
The FDA is recalling all lots of Vista Meibo Tears eye drops due to lack of sterility assurance from manufacturing non-conformance. Approximately 11,520 cartons were distributed nationwide in the USA.
Valley Springs Steamed Distilled Water (1-gallon bottles, UPC 0 31193-00601 2) is recalled because it was bottled under insanitary conditions. The recall affects 263,440 units distributed in Illinois and Wisconsin.
Medline is recalling 291 units of three burn care convenience kit models due to calibration issues with sterilization equipment that may impact product sterility. No illnesses or injuries have been reported.
Asteria Health is recalling one lot of testosterone pellets due to potential presence of metal particulate matter. Affected patients should contact their healthcare provider.