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.
Twin City Foods Inc is recalling Wild Harvest Organic Cut Leaf Spinach due to potential Listeria monocytogenes contamination.
JCB Flavors is recalling Southwestern Seasoning Rub because the ground cumin ingredient tested positive for trace peanut allergens.
Con Yeager Spice Company is recalling Shirks Cajun Andouille spice mix because it may contain undeclared peanuts.
JCB Flavors is recalling 50 lb boxes of Bacon Dip Mix because the ground cumin ingredient tested positive for trace peanut allergens.
Con Yeager Spice Co is recalling Ray's Rub spice mixes because they may contain undeclared peanuts.
Inventure Foods is recalling Rader Farms Fresh Start Smoothie Blend due to potential Listeria monocytogenes contamination. Consumers should check lot codes and best-by dates.
JCB Flavors is recalling specific lots of Curry Powder because the ground cumin ingredient tested positive for trace peanut allergens.
JCB Flavors is recalling Smokey Jo BBQ Rub because the ground cumin ingredient tested positive for trace peanut allergens.
Starcraft is recalling 2015 Prodigy and Quest school buses because seat foam may not meet federal flammability standards, increasing fire risk.
Vapor Bus is recalling ETO Controller Assemblies because a software defect may cause rear passenger doors to open without warning while the bus is moving.
Eldorado National is recalling 2012-2014 Passport HD vehicles because a power cable may chafe and short, increasing the risk of a fire.
Hickory Springs is recalling CE White school bus seat assemblies because the foam may not meet federal flammability standards, increasing fire risk.
Starcraft RV is recalling 36 model year 2016 Launch and AR-One travel trailers because Federal Certification Labels may list the wrong tire size.
IKEA is expanding a recall of SULTAN and VYSSA crib mattresses because gaps between the mattress and crib ends could entrap infants.
Allied Recreation Group is recalling specific Holiday Rambler fifth wheel trailers because the installed microwaves may start on their own, posing a fire hazard.
Felt Bicycles is recalling Deep Six and El Guapo cruiser models because the brakes can fail, posing a crash hazard. No injuries have been reported.
Ohanyan's Inc. is recalling approximately 159,291 pounds of dried beef sausage products because they contain undeclared soy lecithin, a known allergen.
Branded LLC is recalling H-E-Buddy kaleidoscope toys sold at H-E-B stores in Texas because removable end caps expose small parts and internal components that pose choking and laceration risks.
Churchill Medical Systems is recalling 8-inch Standard Bore Extension Sets due to a potential leak caused by insufficient bonding between the needleless device and the female luer.
Churchill Medical Systems is recalling 6,850 units of 7-inch Standard Bore High Pressure Extension Sets due to a potential leak caused by insufficient bonding between the needleless device and female luer.
Attix Pharmaceuticals is recalling all lots of Rebamipide API distributed between January 2012 and February 2015 due to potential penicillin cross-contamination from inadequate facility separation.
Attix Pharmaceuticals is recalling progesterone active pharmaceutical ingredient due to potential penicillin cross-contamination during repackaging.
Attix Pharmaceuticals is recalling paroxetine active pharmaceutical ingredient repackaged between January 2012 and February 2015 due to potential penicillin cross-contamination.
Attix Pharmaceuticals is recalling Bismuth Subcarbonate active pharmaceutical ingredient due to potential penicillin cross-contamination from inadequate facility separation.
Churchill Medical Systems is recalling 450 units of 4-inch Microbore T-Port Sets due to a potential leak caused by insufficient bonding between components.