Hazard
9,610 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 9,610 mis labeling recalls we have scored against our rubric, 161 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 588 (6%) 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 mis labeling 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.
The Popcorn Factory is recalling Dill Pickle Lite Works Popcorn because it contains milk, an allergen not declared on the label.
Bedessee Imports is recalling Brown Betty Coconut Milk Powder Mix because it contains sodium caseinate but lacks a milk declaration.
New Punjab Sweets Inc. is voluntarily recalling Ladoo snacks because they lack an ingredient label and may contain undeclared nuts, colors, and wheat.
Coalescence LLC is recalling Spicy Black Bean Burger powder mix because it contains undeclared peanuts. The product was distributed to consignees in Ohio, Utah, and Michigan.
3M is initiating a field correction to remove the crown indication from all Lava Ultimate products. The products remain indicated for onlays, inlays, and veneers.
RTI Surgical is recalling 25 units of the Songer Spinal Cable System because the box end label incorrectly identifies the material as Titanium instead of Stainless Steel.
Integra LifeSciences is voluntarily recalling 123 Tuohy needles because they were incorrectly labeled as 18 gauge, 3.5 inch instead of 20 gauge, 5 inch.
Bard Access Systems is recalling PowerPICC Solo Catheter Kits because they have incorrect expiration dates on the primary labeling.
Bard Access Systems is recalling PowerPICC Solo Catheter Kits because the primary labels display incorrect expiration dates.
Bard Access Systems is recalling PowerPICC Solo Catheter Kits because the primary labels contain incorrect expiration dates.
Bard Access Systems is recalling PowerPICC Solo Catheter Kits because the primary labels contain incorrect expiration dates.
Volk Optical Inc is recalling 78 units of the Lombart 90D Clear lens due to an incorrect lot number engraved on the aluminum ring.
Boston Scientific is recalling one lot of Extractor Pro RX Retrieval Balloon Catheters because the device contains a syringe size larger than what is identified on the label.
Synthes, Inc. is recalling 276 DePuy Synthes 6.5 mm Titanium Recon Screws because certain lots contain the wrong insert.
Spine Wave, Inc. is recalling 121 Spine Wave Access Kits because the outer carton mislabels the monopolar probe dimensions. The probe is listed as 200 x 1.5mm instead of the correct 280 x 1.5mm.
Vascutek is recalling 12 Gelseal vascular grafts labeled as 30cm but actually 15cm. The devices were distributed in Michigan and four other countries.
RTI Surgical is recalling 18 units of three lots of Bullet-Tip PEEK VBR implants distributed in Florida and New York due to incorrect color labeling.
Vascutek, Ltd. is recalling 12 Gelseal vascular grafts labeled as 30cm but actually 15cm. The devices were distributed in Michigan and four other countries.
Milestone Scientific is recalling 165,850 Wand STA handpieces because they were mislabeled as STA handpieces, which cannot be installed in the STA instrument.
Varian Medical Systems is recalling 46 Leipzig-style Surface Applicator Sets because the actual dose rate is approximately 14% higher than the rate published in the Instructions for Use.
Crystal Fresh is recalling SNOBIZ Cheesecake Shave Ice Flavor due to an undeclared milk allergen. The product was distributed in multiple US states and Canada.
Natural Creations Inc is recalling Glucosamine MSM dietary supplements because they contain an unlabeled shellfish allergen. The recall affects 644 bottles distributed nationwide.
Whole Foods Market is recalling Jivara Lactee Milk Chocolate Valrhona because one retail location failed to declare hazelnuts on the label.
Cook Inc. is recalling 123,184 LapSac Surgical Tissue Pouches because the labeling includes information not stated in the intended use.
Golden Chocolate International is recalling 513 lbs of ROGALIK PAPAYA due to undeclared FD&C food colorings. The product was distributed in New York and Pennsylvania.