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.
SlumberWorld is recalling approximately 810 mattresses sold in Hawaii from 2011 to 2012 because they fail to meet the mandatory federal open flame standard, posing a fire hazard.
Balsam Hill is recalling about 700 pre-lit artificial Christmas trees because the remote control receiver box can overheat and melt, posing burn and shock risks.
Supreme is recalling 2009-2010 Startrans MFSAB school buses with Ricon wheelchair lifts due to a potential fire hazard from an armored cable.
Supreme Corporation is recalling 2006-2012 Startrans buses with Ricon wheelchair lifts because an armored cable may cause a short circuit and fire.
Jerdon Style is recalling about 6,000 one-cup coffeemakers because they can overheat, posing fire and burn hazards. No injuries have been reported.
Nestle USA is recalling Lean Cuisine Mushroom Mezzaluna Ravioli because consumers reported finding small fragments of glass inside the product.
Liberty Mountain is recalling Singing Rock Easy Go XP Lock Via Ferrata Lanyards because the elastic webbing can break, posing a risk of serious injury or death.
Codman & Shurtleff is recalling NeuroPath 6Fx100 Guiding Catheters because package integrity issues may compromise device sterility.
Codman & Shurtleff is recalling NeuroPath 5Fx90 Guiding Catheters because package integrity issues may compromise device sterility.
Codman & Shurtleff is recalling NeuroPath 6Fx100 Guiding Catheters because package integrity issues may compromise device sterility.
Codman & Shurtleff is recalling NeuroPath 5Fx100 Guiding Catheters because package integrity issues may compromise device sterility.
Codman & Shurtleff is recalling NeuroPath 5Fx100 Guiding Catheters because package integrity issues may compromise device sterility.
Codman & Shurtleff is recalling 25 NeuroPath 6Fx100 Guiding Catheters because package integrity issues may compromise device sterility.
Vascular Solutions, Inc. is recalling SuperCross Microcatheters due to potential surface contamination on aged units discovered during in-house testing.
Bimbo Bakeries is recalling specific varieties of Thomas' Bagels because metal fragments were found in two packages. Consumers should check their packages and stop eating them.
Codman & Shurtleff is recalling NeuroPath 5Fx90 Guiding Catheters because package integrity issues may compromise device sterility.
Codman & Shurtleff is recalling NeuroPath 6Fx100 Guiding Catheters because package integrity issues may compromise device sterility. The recall covers 34 units distributed worldwide.
Codman & Shurtleff is recalling NeuroPath 5Fx90 Guiding Catheters because package integrity issues may compromise device sterility.
Varian Medical Systems is recalling 1,168 units of the Eclipse Treatment Planning System because the Pencil Beam Convolution 11.0 algorithm incorrectly calculates dose for dynamic plans with different energy fields.
Codman & Shurtleff is recalling NeuroPath 6Fx100 Guiding Catheters because package integrity issues may compromise device sterility.
Bimbo Bakeries USA is recalling Weight Watchers 6 Original Bagels because metal fragments were found in two packages.
Codman & Shurtleff is recalling NeuroPath 5Fx100 Guiding Catheters because package integrity issues may compromise device sterility.
Codman & Shurtleff is recalling 268 units of Neuropath 6Fx90 Guiding Catheters because package integrity issues may compromise device sterility.
Animas Corporation is recalling insulin infusion pumps that will stop operating on January 1, 2016, due to an internal calendar date limit.
Medrad Inc is recalling Hand Controller Sheaths because a missing seal may compromise sterility. The product is used in cardiac catheterization procedures.