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.
Asher's Chocolate Co is recalling Peanut Butter Coated Mini Pretzels due to potential Salmonella contamination. Consumers should stop eating the product.
Asher's Chocolate Co is recalling White Confectionery Coating due to potential Salmonella contamination. Consumers should check their lot numbers and stop using the product.
Asher's Chocolate Co is recalling Dark Chocolate Almond Paw products due to potential Salmonella contamination. Consumers should check for Lot # 000336473.
BD Diagnostic is recalling BD Viper LT software version 3.00H because it generates lower-than-expected RFU values, which may impact test results.
Zutano is recalling about 38,000 infant Cozie booties because the rubber grips on the bottom can detach and pose a choking hazard.
Chrysler is recalling 2014-2017 Ram ProMaster vehicles because labels incorrectly state they have frontal air bags. This mislabeling may increase injury risk in a crash.
Horizon Hobby is recalling specific ECX model vehicles because the electronic speed control can short circuit and catch fire. No injuries or property damage have been reported.
Ducati is recalling 2016-2017 Multistrada 1200 Enduro motorcycles because the rear shock absorber may crack and detach, increasing crash risk.
Nissan is recalling 2016-2017 Titan Crew Cab vehicles because the rear seatbelt assembly may not adequately protect the occupant's head during a crash.
Forest River is recalling 2017-2018 Prime Time Avenger motorhomes because the Federal Placard incorrectly lists tire specifications, potentially leading to improper tire installation.
Riverside RV is recalling 2017-2018 Mt. McKinley and Whitewater travel trailers because they lack required rear-facing reflectors and reflective tail lights, increasing crash risk.
Razor is recalling about 158,000 RipStik electric motorized caster boards because the rear wheel can lock up, posing a fall hazard.
Conagra Brands is recalling 110,817 pounds of frozen chicken nugget meal trays because the included brownie mix may be contaminated with Salmonella.
Dolcetta Artisan Sweets is recalling 180 boxes of Hot Cocoa Hearts sold in Oregon and Washington due to undeclared soy lecithin.
Dolcetta Artisan Sweets is recalling Hot Cocoa Snowballs because they contain undeclared soy lecithin, a common allergen.
Dolcetta Artisan Sweets is recalling 360 boxes of Salty Caramel Truffles in Oregon and Washington due to undeclared soy lecithin and milk.
Companion Foods Corp. is recalling Braised Bamboo Shoot Tips because wheat is not properly declared in the ingredient list.
ConMed is recalling Hyfrecator 2000 ESU cartons because they were packaged with non-sterile handpiece sheaths labeled as sterile, posing a risk of infection.
GE Healthcare is recalling Vivid Ultrasound systems because slow search times can cause operators to select the wrong patient, potentially leading to misdiagnosis.
Datascope Corporation is recalling 21 custom tubing packs with Bioline coating due to a reported assembly error on the oxygenator line.
Windstone Medical Packaging is recalling 7,508 cataract packs because the sterile packaging of the included eye pads may be compromised.
Dolcetta Artisan Sweets is recalling 30 bags of Milk Chocolate Almond Toffee Tree in Oregon and Washington due to undeclared soy lecithin.
ConMed is recalling Hyfrecator 2000 handpiece sheaths because non-sterile units were packaged in pouches labeled as sterile, posing a risk of infection.
Micromedics, Inc. is recalling 273 units of FibriJet Endoscopic Catheter Introducers because small channels in the sterile packaging seal may compromise package integrity and sterility assurance.
J & J Distributing Company is recalling 7 cases of Detox Salad because shredded carrots used as an ingredient were contaminated with metal pieces.