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.
Amerisource Health Services is recalling specific lots of Chlorpromazine Hydrochloride 25mg tablets nationwide due to detection of a micro-organism in packaging material at the manufacturing site.
Northwind Pharmaceuticals recalls Sulfamethoxazole and Trimethoprim tablets due to microorganism found in packaging material. No microorganism detected on tablets; no illnesses reported.
Amerisource Health Services is recalling Chlorpromazine Hydrochloride 200 mg tablets distributed nationwide due to a micro-organism detected in auxiliary packaging material. The tablets themselves were not contaminated.
Boston Scientific is recalling Encore 26 Inflation Devices due to potential foreign material particles that could migrate into balloon catheters during use. No injuries have been reported.
Zydus Pharmaceuticals is recalling Succinylcholine Chloride Injection due to out-of-specification test results showing unknown degradation impurities. Approximately 270,125 vials were distributed in MS, OH, LA, and Puerto Rico.
The FDA is recalling a specific lot of Sulfamethoxazole and Trimethoprim due to presence of a micro-organism in the auxiliary polyester coil packaging material. No micro-organism was detected on the tablets themselves.
AvKARE is recalling Chlorpromazine Hydrochloride Tablets, USP 50 mg due to the presence of a foreign substance. The recall affects 1512 cartons distributed nationwide.
Amneal Pharmaceuticals recalls specific lots of Chlorpromazine Hydrochloride 25 mg tablets due to a micro-organism detected in packaging material. The medication itself remains uncontaminated.
Onkos Surgical is recalling 30 units of ELEOS BOWED CANAL FILLING STEMS nationwide due to an unidentified substance found during a retrospective evaluation. The substance's impact is unknown.
Diagnostica Stago is recalling STA-Fibrinogen 5 diagnostic kits due to potential contamination that could affect anticoagulation monitoring tests in patients receiving heparin therapy.
Diagnostica Stago is recalling STA-Liquid Anti-Xa diagnostic test kits due to potential contamination from fibrinogen reagents. The kits measure anticoagulant medication levels in clinical laboratories nationwide and internationally.
Reser's Fine Foods is recalling Tuna Salad due to potential Listeria monocytogenes contamination from a recalled ingredient. The affected product was distributed across 29 states.
Aequita Pharmacy is recalling 194 vials of Semaglutide + Cyanocobalamin injectable solution due to lack of manufacturing process controls. The affected product was distributed in Massachusetts.
Remel is recalling Blood/MacConkey Biplate culture media (611 units) distributed nationwide due to potential surface and subsurface contamination with Listeria monocytogenes.
Remel, Inc. is recalling Strep Selective II Agar (371 units) due to potential surface and subsurface contamination with Listeria monocytogenes. Users should contact the manufacturer for instructions.
Medline Convenience Kits containing BD ChloraPrep Clear applicators are being recalled due to potential open seals in packaging that could compromise sterility and lead to infection.
Rich Ice Cream Co is recalling Cotton Candy Twirl Bar frozen novelties due to potential Listeria monocytogenes contamination. The recall affects approximately 110,292 cases distributed across 24 U.S. states and territories.
Dr. Reddy's Laboratories is recalling Omeprazole 20mg capsules due to the presence of foreign Divalproex Sodium 250mg tablets in bottles. No illnesses have been reported.
UNFI General Corporate is recalling Wild Harvest OG2 Cauliflower due to potential contamination with fluid from a reach truck. Affected products were distributed in NJ, NY, MD, DC, and PA.
UNFI General Corporate is recalling Florida Bicolor Sweet Corn and Eastern Bi-Color Tray Pack for potential contamination with reach truck fluid. No illnesses have been reported.
UNFI General Corporate is recalling USA/MEX OG2 Spinach due to potential contamination from reach truck fluid. The recall affects 213 cases distributed in NJ, NY, MD, DC, and PA.
UNFI General Corporate has recalled 213 cases of S.AMERICA OG1 Anjou Pears distributed in NJ, NY, MD, DC, and PA due to potential contamination with fluid from a reach truck. No illnesses have been reported.
UNFI General Corporate is recalling 213 cases of WLD HRVST OG2 lemons distributed in NJ, NY, MD, DC, and PA due to potential contamination with fluid from a reach truck. Consumers are advised to discard affected product.
UNFI is recalling three parsley products (213 cases total) due to potential reach truck fluid contamination. Products were distributed in NJ, NY, MD, DC, and PA.
UNFI General Corporate is recalling celery products that may be contaminated with fluid from a reach truck. Affected products were distributed in New Jersey, New York, Maryland, Washington D.C., and Pennsylvania.