Severity 4 of 5
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.
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.
Nourish Inc. Fruit Snack Pack SNACK ATTACK recalled for undeclared peanut allergen. 188 units distributed to 4 customers in California.
3M is recalling 248,750 Steri-Drape surgical drapes used in medical facilities worldwide. The adhesive liner is difficult to remove without damaging the product, and there are reported increases in adhesive-related skin injuries.
3M is recalling Steri-Drape Large Towel Drapes (REF 1010NS) due to adhesive liner defects that may damage the product and increased reports of adhesive-related skin injuries from affected lots.
3M has recalled 17,200 units of urological drapes due to adhesive liner removal difficulty and reported skin injuries. The affected drapes may become unusable in surgical settings.
Whele LLC is recalling the Mighty Bliss Electric Heating Pad due to burn and shock hazards. The company has received complaints of burns, electrical shocks, and skin irritation.
Umami Everyday Savory Spice is recalled nationwide due to undeclared soy. The product affects consumers with soy allergies and has been distributed in the US, Canada, UK, and France.
Whele LLC is recalling approximately 4,034 Mighty Bliss Electric Heating Pads due to burn and shock hazards. The firm received complaints of burns, mild electrical shocks, and skin irritation.
Kalera butter lettuce (lot #001293 and #001294) is being recalled due to potential Salmonella contamination. Consumers should not consume the affected product.
Kalera recalls Living Hydroponic Baby Romaine Lettuce (lot #001293) due to potential Salmonella contamination. The affected products comprise 211 cases of 10-pound packages distributed domestically.
Wild caught Alaskan Sockeye smoked salmon may be contaminated with Listeria monocytogenes. Seven Seas International USA LLC is recalling 540 cases distributed to 164 retail stores.
3M is recalling 504,000 units of Steri-Drape surgical drapes worldwide because the adhesive liner is difficult to remove and may damage the product. Reported cases of adhesive-related skin injuries have been associated with the affected lots.
3M is recalling 769,810 Steri-Drape surgical drapes worldwide due to a defective adhesive liner that is difficult to remove and has caused reported skin injuries.
3M is recalling Steri-Drape surgical drapes due to a defective adhesive liner that is difficult to remove and may render the drape unusable. Reported adhesive-related skin injuries have been linked to the affected lots.
3M is recalling surgical drapes with defective adhesive components that may cause skin injuries. The adhesive liner is difficult to remove without damaging the product, and increased skin injuries have been reported.
3M is recalling Steri-Drape surgical drapes because the liner on the adhesive component is difficult to remove without damaging the drape. An increase in adhesive-related skin injuries has been reported for affected lots.
3M is recalling 554,200 surgical drapes due to a difficult-to-remove adhesive liner that may damage the product and render it unusable. The company has received reports of adhesive-related skin injuries from the affected lots.
3M is recalling Steri-Drape surgical drapes (large towel drape, REF 1010) distributed worldwide. The affected drapes have reported adhesive-related skin injuries and a liner that is difficult to remove without damaging the product.
Insulet Corporation is recalling the Omnipod Dash PDM remote controller for insulin pumps due to battery defects causing overheating, swelling, and fire hazard. A fire incident has been reported.
Zingerman's Creamery is recalling Paw Paw Gelato in pint (16 oz) and quart (32 oz) sizes due to undeclared egg. Consumers with egg allergies should not consume this product.
Zingerman's Creamery is recalling Harvest Pumpkin Gelato due to undeclared egg allergen. The recall affects pints and quarts distributed in Michigan.
Polaris is recalling approximately 138,000 snowmobiles from model years 2013–2023 because electrostatic discharge inside the fuel tank can cause vapors to ignite, leading to tank burst and fire. The firm has received 30 reports of tank bursting, including 16 fires and one burn injury.
Whole Foods Market Dipping Caramel (PLU 34888) is recalled because it contains wheat that was not declared on the label. Consumers with wheat allergies should not consume this product.
CooperSurgical is recalling NEO-fit Neonatal Endotracheal Tube Grips due to metal clips that can become loose or detach. Eleven complaints include three cases of clip ingestion, three removals from the mouth, and one throat laceration.
Albertsons Companies LLC is recalling Chicken Salad Sandwich Club trays because labels fail to disclose tree nuts (cashews) in the ingredient and contains statements. Consumers with cashew allergies may unknowingly consume these sandwiches.
DA CHENG VEGETARIAN FOOD INC. recalls Vegan Golden Nuggets due to undeclared egg allergen. The product is marketed as vegan but contains egg, which is not declared on the label.