Hazard
203 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 improper storage 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.
UDENYCA (pegfilgrastim-cbqv) injection is being recalled because 116 cartons of Lot 2199821 were stored at room temperature instead of required refrigerated conditions.
Gelson's hummus products are being recalled due to missing refrigeration storage instructions on the label. Affected consumers should verify their lot codes and take appropriate precautions.
XOLAIR (omalizumab) injectable is being recalled due to exposure to temperatures outside its labeled storage requirements. The affected lot (3617756) was distributed nationwide. Patients should contact their healthcare provider regarding their supply.
Abbott Rapid DX diagnostic control products were improperly stored during transit due to severe thunderstorms, which may cause inaccurate or delayed test results.
Abbott hepatitis B diagnostic reagent stored outside recommended conditions due to transit delays from severe thunderstorms. Improper storage could result in inaccurate or delayed test results.
Ortho Clinical Diagnostics VITROS BUN reagent distributed nationwide may have been stored outside recommended conditions during transit due to severe thunderstorms, potentially causing incorrect or delayed test results.
Ortho Clinical Diagnostics' VITROS Calcium reagent (300-pack) is being recalled due to transit delays from severe thunderstorms that may have exposed the product to temperatures outside recommended storage conditions, potentially affecting test accuracy.
A Sekisui Diagnostics HCG control set used in clinical laboratories may have been exposed to improper storage temperatures during transit due to severe thunderstorms. This exposure could result in incorrect or delayed test results.
Abbott diagnostic calibrators may have been stored improperly during transit delays caused by thunderstorms, potentially affecting test accuracy. The units are being recalled to prevent inaccurate or delayed diagnostic test results.
Mckesson Medical-Surgical Inc. is recalling VITROS phosphorus reagent due to improper storage during transit caused by severe thunderstorms. The storage deviation could affect test result accuracy.
BD Microbiology MAC Conkey II Agar culture media was exposed to improper storage conditions during transit due to severe thunderstorms. This may cause inaccurate or delayed test results.
Medline Industries is recalling one lot of Meridian ImmunoCard STAT! Crypto/Giardia Test Kits due to improper temperature storage. The affected lot was distributed nationwide.
Cardinal Health is recalling Wegovy (semaglutide) injection due to potential temperature exposure during shipping. Product was stored outside labeled refrigeration conditions due to a distribution center error.
AKT Trading Inc. is recalling Menma Ajitsuke prepared bamboo shoots because the packaging is missing a "Keep Refrigerated" statement. The product requires refrigeration and improper storage could allow bacterial growth.
Target Corporation recalled Nestle Toll House Valentine's Chocolate Chip cookie dough (UPC 028000344085) due to improper storage temperature. The product was distributed in AK, CA, ID, MT, OR, and WA.
Pacific Shellfish, Inc. is recalling Signature Blue Swimming Crab Claw and Lump canned crab (lots #78821 and #788454) from California due to storage at temperatures above 40°F without ice as of July 1, 2024.
Baxter Healthcare's Infuvite Adult Multiple Vitamins Injection is being recalled because 70 vials were stored outside their labeled specifications, potentially affecting product stability. The affected vials were distributed to three direct accounts in Arizona, New Mexico, and Utah.
McKesson Medical-Surgical is recalling Rocuronium Bromide Injection vials due to storage outside label specifications. Seventy vials were distributed to three healthcare accounts in New Mexico, Arizona, and Utah.
Mckesson is recalling Bicillin L-A prefilled syringes stored outside label specifications. The FDA Class II recall affects 70 vials distributed to direct accounts in NM, AZ, and UT.
CABTREO acne medication was stored outside refrigeration requirements. The recalled lot was kept at room temperature instead of required refrigerated conditions.
Sopra Ricotta Amalfi manufactured by Greco Sidari is recalled because the product was not held at appropriate temperatures. Improper storage could allow spoilage and pathogen growth.
Greco Sidari is recalling Norpaco Sweetie Pepper Goat Cheese (1,375 cases, 1/5# units) distributed in Ohio, New York, and Pennsylvania. The cheese was not held at appropriate temperatures, which could support pathogen growth.
Greco Sidari is recalling Grande Burrata cheese due to improper temperature storage that could support pathogen growth. The affected products were distributed across Ohio, New York, and Pennsylvania.
Grande Ricotta Sopraffina (1375 cases) distributed across Ohio, New York, and Pennsylvania from November 2023 to January 2024 is recalled because it was not held at appropriate temperatures, which could support pathogen growth.
Sandoz Inc is recalling Enoxaparin Sodium Injection (batch SAH06821A) nationwide due to CGMP deviations: products were exposed to temperatures outside labeled storage conditions, potentially affecting drug stability.