Hazard
256 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 mislabeling 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.
Allison Medical is recalling 150,000 InControl insulin syringes distributed in Texas due to incorrect package labeling of needle gauge. The mislabeled packages may lead patients to unknowingly select the wrong needle size.
Zingerman's Creamery is recalling Paw Paw Gelato in pint (16 oz) and quart (32 oz) sizes due to undeclared egg. Consumers with egg allergies should not consume this product.
Sonendo Inc is recalling 15 GentleWave System APM Procedure Instruments (Model GW-APM-PI02) due to erroneous unit carton labels. The instruments were distributed worldwide, including Ohio and Canada.
DA CHENG VEGETARIAN FOOD INC. recalls Vegan Golden Nuggets for containing undeclared egg. The product was distributed to restaurants and retail stores in Utah, Virginia, Texas, and California.
Bella Cucina Artful Food Sweet Pepper Pesto is being recalled because the label does not declare milk as an ingredient. Consumers with milk allergies could experience a serious allergic reaction.
Medline recalls Adult Blood Culture Collection Kits due to incorrect expiration dates on kit components. The expiration dates on the CHG Solution and Bactec bottle plastic do not match the dates listed on the kit packaging.
Flowers Foods is recalling Tastykake Glazed Cherry Pie due to undeclared soy lecithin in the product. The recalled product may pose a health risk to consumers with soy allergies.
Karlsburger Kitchens NSLP 140 Turkey Gravy Mix labeled as gluten-free contains undeclared gluten. The product was distributed in Kansas, Minnesota, Nebraska, and Wisconsin.
Hobbs Medical, Inc. is recalling Grasping Forceps due to incorrect expiration dates on device labels. Affected devices may be used beyond their safe shelf life if the mislabeled expiration dates are not corrected.
Hobbs Medical is recalling Posi-Stop Injection Needles (lot numbers ending in R) due to incorrect expiration dates on labels that extend shelf life. Affected devices were distributed in the US from March 2018 to September 2020.
Hobbs Medical is recalling Freeman Pancreatic Flexi-Stents with incorrect expiration dates on device labels that extend shelf life. Devices were distributed in the US and internationally from March 2018 to September 2020.
Hobbs Medical recalled 10 units of its Helical Retrieval Basket due to mislabeled expiration dates that extend the product's shelf life, affecting devices distributed in the US and select countries between 2018 and 2020.
Hobbs Medical is recalling Polypectomy Snare devices (Catalog Number 4564) due to incorrect expiration dates on labels that extend the stated shelf life. The 35 affected units, distributed in the US and select countries, may be used beyond their actual safe shelf life.
Hobbs Medical is recalling the Freeman Pancreatic Flexi-Stent Kit because the device label displays an incorrect expiration date that extends the shelf life. U.S. distribution of affected devices occurred between March 25, 2018 and September 28, 2020.
Hobbs Medical is recalling Helical Retrieval Baskets due to incorrect expiration dates on device labels. The mislabeling extends the shelf life, potentially allowing use of expired devices.
Hologic recalls 233 BioZorb LP Markers nationwide due to removable labels showing incorrect expiration dates. Implants labeled with January 2022 dates may be mistakenly used after their actual July 2024 expiration.
Teva Pharmaceuticals is recalling 83,703 bottles of prescription amphetamine tablets nationwide because bottles labeled as 15 mg strength actually contain 20 mg tablets, creating risk of unintended overdose. Patients should contact their pharmacy or healthcare provider.
GNC Vitamin B-6 100mg dietary supplement bottles actually contain Pycnogenol due to a filling line error. The product was distributed across all 50 US states and multiple international locations.
Charlie's brand Spinach Salad With Honey Dijon Dressing is recalled due to undeclared fish (anchovy) in the Worcestershire sauce dressing. Consumers with fish allergies are at risk.
PICS Ground Cinnamon distributed to Price Chopper stores in Massachusetts is being recalled because the product actually contains cumin but is mislabeled as cinnamon.
FDA recalls 8 SteriSpine PS multi-axial fenestrated screw kits distributed in Maryland due to incorrect labeling on patient documentation. The patient labels list the wrong screw type, though other labeling and the devices themselves are correct.
Wolf-Pak Premium Dressing Kits labeled latex-free are being recalled because a component contains natural rubber latex, posing a risk to people with latex allergies.
Trinity Sterile's IV catheter dressing trays are mislabeled as latex-free despite containing natural rubber latex in component 94-7002, risking allergic reactions in latex-sensitive users.
The FDA has recalled Dose Vital VIP Products Vital Honey With Caviar and Tongkat Ali Powder due to undeclared Tadalafil. The product was distributed in seven states and poses serious health risks.
Boston Scientific is recalling 10 EkoSonic Endovascular Device Kits due to mislabeling. The affected kits were distributed to healthcare facilities in 10 U.S. states.