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.
Volvo Trucks is recalling 2018-2020 VAH, VHD, VNL, and VNR models because a fuse may blow, preventing the transmission from shifting and increasing crash risk.
SRAM is recalling RockShox Lyrik and Yari front suspension forks because the lower leg assembly can break, causing riders to lose control and crash.
Nova Bus is recalling 2014-2017 LFS and LFS Artic buses because improperly tightened seat hardware may cause cantilever seats to drop, increasing injury risk.
Faraday is recalling about 4,450 electric bicycles because the seat posts can break, posing a fall hazard to riders.
Thor Motor Coach is recalling 1,554 motorhomes because a software defect may cause slide-out rooms to move unexpectedly, increasing injury risk.
Toyota is recalling 2017-2019 Camry, Corolla, RAV4, Sienna, and Yaris iA vehicles because an incorrect load capacity label may lead to unintentional overloading.
Dolan Northwest is recalling Design Classics chandeliers because the top loop can break, causing the fixture to fall and pose impact and laceration risks.
Mazda is recalling 262,220 vehicles due to a software error that may cause the engine to stall unexpectedly, increasing crash risk.
Gillette is recalling Venus Simply3 disposable razors because manufacturing errors caused blade misalignment, posing a risk of cuts during normal use.
Fisher-Price is recalling inclined sleeper accessories for Ultra-Lite Day & Night Play Yards due to safety concerns about infant sleep on inclined surfaces.
BRP is recalling Sea-Doo marine coolers because the latch can lock automatically, posing entrapment and suffocation risks. No injuries have been reported.
Wismettac Asian Foods is recalling 40 units of Monaka Belgium Choco & Kurumi Daiichi F in California because the product does not declare coconut as an ingredient or allergen.
GE Healthcare is recalling 1,113 Discovery PET/CT 710 systems because the table may stop moving without stopping X-ray exposure.
GS Fireworks is recalling 26 types of consumer fireworks sold in Wyoming, Michigan, because they are overloaded with pyrotechnics, posing explosion and burn risks.
MOWI USA LLC is recalling 35 lb cases of Atlantic Salmon because samples tested positive for Listeria monocytogenes. The product is non-ready to eat and must be cooked before consumption.
APS BioGroup is recalling Viralox Immune Balancing Polypeptide Oral Spray because testing found elevated levels of Stenotrophomonas maltophilia bacteria.
Zydus Pharmaceuticals is recalling Pramipexole Dihydrochloride Tablets 0.125 mg due to cross-contamination caused by a cleaning failure.
Stryker GmbH is recalling 447 Endotrac ECTR Hook/Triangle Blade Kits because the sterile bag seal may be compromised, potentially affecting sterility.
Renaissance Food Group LLC is recalling 365 by Whole Foods Market Smoked Mozzarella Pasta Salad in Texas, Louisiana, and Oklahoma due to undeclared soy.
Bedessee Imports is recalling National Heartland Naturals Pearl Barley because it was mistakenly labeled gluten-free despite containing gluten.
Gertrude Hawk Brands is recalling R.H. Macy & Co. Milk Chocolate Covered Pecan Caramel Clusters because the packaging failed to disclose the presence of almonds and pecans.
Regal Food Inc. is recalling Cornflake flavor Fundraising Cookies because FDA inspection found undeclared wheat, soy, and milk allergens.
Jerr-Dan is recalling 2018-2019 Heavy Duty Wreckers because the remote control system may cause the engine to shut down unexpectedly, increasing crash risk.
GE Healthcare is recalling 1,113 Discovery PET/CT 610 systems because the table may stop moving while X-ray exposure continues.
Renaissance Food Group LLC is recalling 365 by Whole Foods Market Traditional Egg Salad because it contains undeclared soy.