Severity 4 of 5
The hazard poses a serious risk of illness, injury, or structural failure. 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.
Northwest Wild Products is recalling canned fish and razor clams with codes starting with OC due to potential Clostridium botulinum contamination.
Mylan Institutional, Inc. is recalling Amlodipine Besylate Tablets, 5 mg, because they were produced and distributed with active ingredients not manufactured according to Good Manufacturing Practices.
Northwest Wild Products is recalling various canned seafood products due to potential Clostridium botulinum contamination.
Idle Free Systems is recalling 507 Auxiliary Power Units with Reefer-type trailer Link Kits manufactured between 2010 and 2016. The battery positive cable may short to ground, increasing the risk of a fire.
Kovatch Mobile Equipment is recalling 56 KME fire trucks because replacement driveshafts may twist and fail, potentially immobilizing the vehicle.
Halcore Group is recalling 2013-2016 Horton ambulances because a poorly sealed air conditioner wire harness allows water entry, creating a risk of electrical fire.
Ford is recalling 2013-2015 Taurus, Flex, MKS, and MKT vehicles because a fuel pump component may overheat, causing the engine to stall or preventing the vehicle from starting.
Whirlpool is recalling about 15,200 microwave hood combinations because internal arcing can ignite plastic components, posing a fire hazard.
Hydroblend Inc. is recalling Tortilla Crusted Crumb due to potential contamination with E. coli O121. The product was distributed in Washington state.
Oregon Potato Company is voluntarily recalling IQF 1/4" Frozen White Onion Dice due to potential Listeria monocytogenes contamination.
Oregon Potato Company is voluntarily recalling specific lots of frozen yellow onion dice due to potential Listeria monocytogenes contamination.
Oregon Potato Company is voluntarily recalling fresh white onion dice due to potential Listeria monocytogenes contamination. The product was distributed across multiple US states, Canada, and Ireland.
Nu Life Market LLC is recalling Sun Life Natural Sunflower Kernel Paste because it may be contaminated with Listeria monocytogenes.
Oregon Potato Company is voluntarily recalling 3/8" Frozen Yellow Onion Dice due to potential Listeria monocytogenes contamination. The product was distributed in 17 US states, Canada, and Ireland.
Oregon Potato Company is voluntarily recalling IQF 3/4" Yellow Onion Dice due to potential Listeria monocytogenes contamination.
Domino Foods is recalling 50 lb bags of Pure Cane Large Grain Granulated Sugar due to the presence of metal fragments.
Golden State Medical Supply Inc. is recalling specific lots of Venlafaxine Hydrochloride Extended-Release Capsules, 150 mg, due to failed dissolution specifications.
Nu Life Market LLC is recalling Sun Life Enjoy Life Sunflower Spread because it may be contaminated with Listeria monocytogenes.
Medtronic is recalling Valleylab Laparoscopic Flat L-Hook Electrodes due to a potential sterile barrier breach. The recall covers 119,770 units distributed worldwide.
Oregon Potato Company is voluntarily recalling IQF 3/8" Un-Blanched Yellow Onion Dice due to potential Listeria monocytogenes contamination.
Newly Weds Foods Inc is recalling bulk flour bland breader contaminated with E. coli O121. The product was distributed nationwide in 15, 30, and 50 lb bags or boxes.
Medtronic is recalling Valleylab Laparoscopic Wire L-Hook Electrodes due to a potential sterile barrier breach. The recall covers 50,055 units distributed worldwide.
Oregon Potato Company is voluntarily recalling specific lots of frozen yellow onion strips due to potential Listeria monocytogenes contamination.
Oregon Potato Company is voluntarily recalling fresh white onion strips due to potential Listeria monocytogenes contamination.
Jumping Jack is recalling 2014-2015 utility trailers because a small torsion arm may detach, causing loss of stability and increasing crash risk.