Severity 3 of 5
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.
The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.
Tiffin is recalling 2013 Allegro Bus vehicles because seat belts may be incorrectly attached and fray, reducing their strength and increasing injury risk in a crash.
Koogee-Queen Anne, LLC is recalling Black Raspberry Chip Ice Cream because bulk product lacked labels declaring direct allergens and facility processing of peanuts, tree nuts, wheat, milk, and eggs.
Koogee-Queen Anne, LLC is recalling Raspberry Lemonade Sorbet because the product lacked required ingredient and allergen labels, including facility processing information.
Koogee-Queen Anne, LLC is recalling Caramel Apple Swirl Ice Cream because the bulk product lacked labels declaring direct allergens and facility processing information.
Koogee-Queen Anne, LLC is recalling The Doctor's Cure Ice Cream because bulk product lacked labels declaring direct allergens and facility processing information.
Koogee-Queen Anne, LLC is recalling Dulce de Leche de Salte Ice Cream because the product lacked required ingredient and allergen labels.
Nantucket Distributing is recalling resin wicker outdoor patio set chairs because the rear legs can break, posing a fall hazard. No injuries have been reported.
Oregon Freeze Dry is recalling Mountain House Scrambled Eggs with Ham and Peppers due to undeclared wheat, soy, and coconut, and potential mislabeling as Granola.
Koogee-Queen Anne, LLC is recalling 7 units of Policeman's Special Ice Cream because the bulk product lacked labels declaring direct allergens and facility processing information.
Koogee-Queen Anne, LLC is recalling Chocolate Bourbon Ice Cream because the product lacked required ingredient and allergen labels.
Koogee-Queen Anne, LLC is recalling Peanut Butter Cow Tracks Ice Cream because bulk product lacked labels declaring direct allergens and facility processing information.
Koogee-Queen Anne, LLC is recalling Cinnamon Ice Cream because the bulk product lacked labels, failing to declare direct allergens and facility processing information.
Koogee-Queen Anne, LLC is recalling Shirley's Red Velvet Cake with White Chocolate Icing Ice Cream because the product lacked required ingredient and allergen labels.
Koogee-Queen Anne, LLC is recalling German Chocolate Cake Ice Cream because bulk product lacked labels declaring direct allergens and facility processing information.
Koogee-Queen Anne, LLC is recalling Green Tea Ice Cream because the product lacked required ingredient and allergen labels.
Vascular Technology, Inc. is recalling 164 Mizuho disposable Doppler probes because the sterile barrier was penetrated, potentially rendering the product unsterile.
Zimmer, Inc. is recalling M/L Taper Hip Prostheses with Kinectiv Technology because black residue was observed in the sterile pouches.
Koogee-Queen Anne, LLC is recalling Candy Cane Lane Ice Cream because the product lacked required ingredient and allergen labels.
Koogee-Queen Anne, LLC is recalling Pretzel Logic Ice Cream because the bulk product lacked labels declaring direct allergens and facility processing information.
Koogee-Queen Anne, LLC is recalling Sorghum & Grits Ice Cream because the product lacked required ingredient and allergen labels, including facility processing warnings.
Karl Storz Endoscopy is recalling 968 Essential NEO audio/visual integration units because the connected power cable could overheat, generate smoke, and cause the peripheral to stop working.
Koogee-Queen Anne, LLC is recalling Tiramisu Ice Cream because bulk product lacked labels, failing to declare direct allergens and facility processing information.
Cenorin is recalling 25 HLD System Model 610 units because a temperature sensor defect may prevent water from heating during pasteurization.
The FDA is recalling 264 Devon Supine, Lithotomy and Trendelenburg Positioning Kits because straps may separate from the foam pad.
Koogee-Queen Anne, LLC is recalling Old 502 Sangria Ice Cream because the product lacked required ingredient and allergen labels.