Hazard
41 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 41 missing label recalls we have scored against our rubric, 2 (5%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2 (5%) 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 missing label 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 Regent, Inc. is recalling Levocarnitine Injection USP (1 g/5 mL) due to missing labeling on certain lots. The affected product was distributed nationwide.
Greenpower is recalling 2020-2024 Nano Beast and 2021-2024 Beast school buses because a warning label on the cross-view mirror may be missing, potentially increasing crash risk.
Mobius Imaging is recalling 26 detachable 10in pendant upgrade components for the AIRO CT X-ray System because they do not carry the Safe Hand Position Warning label.
Mobius Imaging is recalling 101 detachable 10in pendant replacement components for the AIRO CT X-ray System because they do not carry the Safe Hand Position Warning label.
GE Medical Systems is recalling 1,818 Senographe Pristina mammography systems because some have a missing or incorrect X-Ray Warning label.
Egress Capital Partners is recalling 3,547 cases of Taproom Gourmet 20 lb bulk Park Mix because the product has no ingredient label and contains six undeclared allergens.
Egress Capital Partners is recalling 3,547 cases of Taproom Gourmet 18 lb bulk Empire Mix because the product has no ingredient label and contains undeclared tree nuts.
Egress Capital Partners is recalling 3,547 cases of Taproom Gourmet 15 lb bulk Madison Mix because the product has no ingredient label and contains undeclared peanuts, almonds, wheat and soy.
El Rojo Wholesale is recalling 2,904 units of El Rojo Pasta De Harina wheat pellets because the pack has no ingredient list, leaving wheat and Yellow No. 6 undeclared.
Egress Capital Partners is recalling 3,547 cases of Taproom Gourmet 15 lb bulk Broadway Mix because the product has no ingredient label and contains undeclared peanuts, sesame, wheat and soy.
Egress Capital Partners is recalling 3,547 cases of Taproom Gourmet bulk Fifth Avenue Mix because the product has no ingredient label and contains undeclared peanuts, almonds, cashew and soy.
Apic Yamada WCM series molding equipment, model WCM-330GL-i, is being recalled because certain products may be out of compliance with FDA electronic product regulations for not bearing a required label. 6 units affected.
Baxter Healthcare Corporation is recalling 60,594 units of Regadenoson Injection nationwide due to missing label information on affected lot numbers. Healthcare providers with affected lots should contact the manufacturer for replacement supplies.
GM is recalling certain 2024 Buick Envision vehicles because they are missing the label stating tire size, pressure and loading information, failing FMVSS 110.
Certain 2025 Hyundai Tucson vehicles may lack glove box airbag warning labels that inform drivers of risks to infants and children in the front seat. Hyundai will mail replacement labels at no cost.
Aurohealth LLC is recalling Acetaminophen, Aspirin and Caffeine tablets because some bottles are missing the manufacturer's label containing drug facts information. Affected product was distributed in NJ, NY, and PA.
Beckman Coulter is recalling Access Substrate reagent bottles (REF 81906) due to missing product labels on certain manufacturing lots. While the missing labels may delay patient test result reporting, no incorrect results have been reported.
Philips has recalled certain surgical C-arm imaging systems delivered to Puerto Rico because they lack required warning labels and are missing a critical Source-to-Skin Distance Spacer component.
Baxter Healthcare Corporation recalls Bendamustine Hydrochloride injection nationwide because labels are missing or partially peeled off vials, raising the risk of medication errors.
Titan Bus is recalling 2017-2021 SRW and DRW school buses because a warning label may be missing from the Cross View Mirror, potentially increasing crash risk.
XO Marshmallow Limited Edition Banana Puddin' OMG is being recalled for missing product labels on packaging. The recall affects 526 retail units distributed in 27 U.S. states and internationally.
Mylan Pharmaceuticals is recalling Insulin Glargine prefilled pens (lot BF21002895) distributed nationwide because some pens lack labels, which could prevent patients from properly identifying and administering the medication.
Procter & Gamble is recalling Crest 3D White Fluoride Anticavity Toothpaste because some tubes lack labels and contain a different formulation than indicated. About 1,128 tubes distributed in Washington State are affected.
Yamaha is recalling about 3,500 Model Year 2021 and 2022 Kodiak 700 ATVs because they are missing the "Maximum Loading Limit" label, which can result in unsafe trailer towing and crash hazards.
Mylan Pharmaceuticals is recalling 89,665 vials of Insulin Glargine Injection (100 units/mL) due to missing labels on the vials. Affected patients should not use the product and should contact their healthcare provider.