Hazard
9,611 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 9,611 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 589 (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.
Aidapak Services is recalling Isosorbide Dinitrate ER tablets because they may be mislabeled as Cilostazol. Patients should check their medication labels.
Aidapak Services, LLC is recalling Hydralazine HCL 25 mg tablets because they may be mislabeled as Docusate Calcium 240 mg capsules.
Aidapak Services, LLC is recalling 1,199 tablets of Cholecalciferol 400 units because they may be mislabeled as other medications.
Aidapak Services, LLC is recalling Pyridoxine HCL 50 mg tablets because they may be mislabeled as other medications. The repacked drugs were distributed in four western states.
Aidapak Services, LLC is recalling Lactobacillus GG capsules because they may be mislabeled as guaiFENesin ER tablets. The repacked drugs were distributed in four western states.
B. Braun Medical Inc. is recalling 19,572 bags of 0.45% Sodium Chloride Injection because the bar code incorrectly identifies the product as Potassium Chloride.
Truitt Brothers Inc. is recalling approximately 1.77 million pounds of Kraft Velveeta Cheesy Skillets Singles Ultimate Cheeseburger Mac due to misbranding and undeclared soy allergens.
Huong Duyen Meat Products is recalling approximately 130,000 pounds of beef and pork products because they contain undeclared wheat, a known allergen.
Cloverdale Foods is recalling approximately 2,664 pounds of beef franks because the label fails to declare milk, a known allergen. No adverse reactions have been reported.
Siemens is recalling HbA1c Flex reagent cartridges due to positive bias and frequent out-of-range flags, which may affect diabetes monitoring.
HP Hood LLC is recalling Hood brand Fat Free Chocolate Milk, 8 oz., because the product was labeled with an extended sell by date.
The Anspach Effort, Inc. is recalling MCA Micro Curved Attachments and cutting burrs because the directions for use do not clearly specify intended use for delicate bone in otologic procedures.
SpineFrontier, Inc. is recalling 13 PedFuse Bone Probes used for spinal pedicle fixation because they were manufactured and marked to incorrect specifications.
RTI Surgical is recalling 1,906 C-Plus 10mm x 12mm Webless implants because they were incorrectly documented as meeting labeling requirements for a partial Vertebral Body Replacement Device.
Mutual Pharmaceutical is recalling specific lots of Fenofibric Acid tablets because the patient insert contains incorrect medical advice regarding HDL-C levels.
Mutual Pharmaceutical is recalling specific lots of Fenofibric Acid tablets because the patient insert contains incorrect medical advice regarding HDL-C levels.
Mutual Pharmaceutical is recalling FIBRICOR (fenofibric acid) tablets because the patient insert contains incorrect medical advice regarding HDL-C levels.
Zimmer is recalling specific lots of medical devices because they were packaged in incorrect outer cartons, though the product labels are correct.
Zimmer is recalling specific lots of hip and shoulder devices due to incorrect outer packaging. Product labels are correct, but the outer cartons were wrong.
Synthes USA HQ, Inc. is recalling 290 Electric Pen Drive Hand Switches because the 'on' and 'lock' labels were interchanged.
Zimmer is recalling specific CPT Hip System parts because they were packaged in the wrong outer cartons, though the product labels are correct.
Coca Cola Bottling Company United-East, LLC is recalling 398 cases of 2-liter Diet Coke that may contain regular Cherry Coke with sugar.
Hahn, Harry O Seafood Inc is recalling Adelphia Seafood Shrimp & Scallop Rotini because Red #40 color additive in the shrimp was not declared on the label.
Philips is recalling 93 HeartStart MRx Monitor/Defibrillators because the first therapy energy setting is mislabeled as 10 instead of 1-10.
Instrumentation Industries Inc. is recalling 220 units of the RTC 25-C Inline Aerosol Tee Adapter because some packages were shipped with incomplete installation and usage directions due to a printing error.