Hazard
20 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 20 chemical residue recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) 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 chemical residue 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.
American Contract Systems Inc is recalling 36 units of Hand Pack procedure kits due to ethylene oxide and ethylene chlorohydrin residuals in the cast padding component exceeding regulatory limits.
American Contract Systems Inc is recalling 26 TOTAL KNEE Procedure Kits due to excess ethylene oxide and ethylene chlorohydrin residues on the cast padding component that exceed safe exposure limits.
American Contract Systems Inc is recalling 129 units of ARTHO KNEE BAPTIST SOUTH PACK Procedure trays (lot numbers 953241, 882241) due to ethylene oxide and ethylene chlorohydrin sterilization residuals exceeding safe limits for permanent-contact medical devices.
American Contract Systems recalls HAND PACK-Procedure Kits due to excess ethylene oxide and ethylene chlorohydrin residuals on the cast padding component, exceeding safe permanent-contact exposure limits.
Peak Harvest salad kits are being recalled because an incorrect foam detergent was used during the vegetable washing process. The recall affects products distributed across 12 U.S. states.
Dole Fresh Vegetables is recalling Marketside Avocado Ranch Chopped Salad Kit due to an incorrect chemical used in the washing process. The product may contain foam detergent residue.
Dole Fresh Vegetables Inc is recalling 6,451 cases of Dole Chopped Kit Chipotle & Cheddar salad kits because an incorrect foam detergent was added to vegetable wash systems, potentially leaving residue on the product.
Dole Fresh Vegetables is recalling certain Chopped Kit salads because an incorrect foam detergent was used in the vegetable wash system. The recall affects approximately 6,451 cases distributed to 12 U.S. states.
American Contract Systems recalls ACS Cath Lab Packs distributed in IL, MO, NE, and TX because they were sterilized with higher than specification ethylene oxide concentrations.
Karl Storz Endoscopy is recalling sterile insufflation tubing because it may contain higher ethylene oxide residues than the acceptable level.
Terra Ingredients is recalling Organic Gold and Brown Flax due to the detection of the chemical residue Haloxyfop.
Heartland Catfish Company is recalling approximately 69,016 pounds of fresh and frozen catfish products that may be adulterated with leucomalachite green, a residue of public health concern.
ConForMIS is recalling iDuo Bicompartmental Knee Replacement Systems due to potential small amounts of ethylene glycol residue.
ConforMIS is recalling 110 units of the iTotal Posterior Stabilized Knee Replacement System because they may contain small amounts of ethylene glycol residue.
ConforMIS, Inc. is recalling 3 units of the iTotal CR Knee Replacement System because they may contain small amounts of ethylene glycol residue.
ConforMIS, Inc. is recalling 71 units of the ConForMIS Unicondylar Knee Replacement System iUNI G2, Left Medial due to potential small amounts of ethylene glycol residue.
ConForMIS is recalling 6 units of the iUNI Unicondylar Knee Replacement System due to potential ethylene glycol residue.
Harvest Sensations LLC is recalling Verdex Fresh Snow Peas due to unapproved fungicide residue detected in a random sample.
Restoration Robotics is recalling ARTAS hair restoration kits because skin tensioner pins contain iron and chlorine residue from insufficient cleaning.
Cooper Vision is recalling 246 units of AVAIRA Toric Contact Lenses because they exceeded the acceptance limit for silicone oil residual.