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.
Jenis Splendid Ice Creams LLC is recalling Strawberry Rose Petal frozen dessert because the product labeling does not include ingredients.
Jenis Splendid Ice Creams LLC is recalling Pineapple Yogurt frozen dessert because the product labeling does not include ingredients.
Jenis Splendid Ice Creams LLC is recalling Torrone frozen dessert because the packaging does not list ingredients, posing a risk to consumers with allergies.
Jenis Splendid Ice Creams LLC is recalling Cassis Sorbet because the frozen dessert labels do not list ingredients. The product was distributed to all 50 states.
Jenis Splendid Ice Creams LLC is recalling Strawberry Sorbet because the frozen dessert lacks ingredient information on the label.
Jenis Splendid Ice Creams LLC is recalling Dark Cocoa Smoked Almond frozen desserts because the packaging does not list ingredients.
Jenis Splendid Ice Creams LLC is recalling Apple Cider Sorbet because the frozen dessert packaging does not list ingredients.
B. Braun Medical is recalling AccuFlo infusion devices in Missouri due to a mismatch between inner and outer packaging labels.
Teleflex Medical is recalling sterile soft rubber bladder catheters because the product labels failed to include a Natural Rubber Latex caution statement.
Jenis Splendid Ice Creams LLC is recalling Heirloom Melon Sorbet because the frozen dessert labels do not list ingredients.
Jenis Splendid Ice Creams LLC is recalling Backyard Mint Straciatella frozen dessert because the product labeling does not include ingredients.
Amerx Health Care Corp. is recalling Amerigel Daily Dressing Advanced 3-in-1 Hydrogel because the product labeling includes unapproved claims for antimicrobial and autolytic debridement.
Siemens Healthcare Diagnostics is correcting ADVIA Centaur and XP systems where improperly loaded sample racks may cause sample ID misreads.
Jenis Splendid Ice Creams LLC is recalling Winter Squash with Pecan Pralines frozen dessert because the packaging does not list ingredients.
Jenis Splendid Ice Creams LLC is recalling Savannah Buttermint frozen dessert because the packaging does not list ingredients.
Advanced Photonic Systems is recalling 235 Photonica Light Modulator units because they were marketed without FDA clearance or approval.
Solace International is recalling Dermatend Original mole and wart remover because the label contains unapproved claims. The product is not FDA approved.
Amerx Health Care Corp. is recalling Amergel Wound Dressing Maximum Strength because the product labeling contains unapproved claims regarding antimicrobial and autolytic debridement properties.
Diagnostica Stago is recalling 514 Liquid Anti-Xa kits due to customer complaints about barcode misreading on analyzers.
Becton Dickinson is recalling 585,048 BD MAX MRSA Assay tests because some samples yielded false positive results during CAP surveys.
Concentric Medical Inc is recalling nine Merci Retriever devices shipped past their expiration date. The devices were labeled with the correct expiration date but distributed to US customers after that date.
Grace Foods (USA) Inc is recalling Grace Classic Coconut Milk cans due to a label misprint that incorrectly states no gums, thickeners, or stabilizers were added.
Biomet 3i is recalling 6 units of Bellatek Encode Healing Abutments because the labels have incorrect color coding, though the identifiers are correct.
Roche Diagnostics is recalling 148 cobas IT 1000 devices because they may assign test results to the wrong patient ID if specific system messages are received.
American Honda is recalling 2014 EU7000isN AT generators because the rear frame support can fail during lifting, posing an impact hazard. The owner's manual may also contain errors.