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.
Forest River is recalling 2017 Prime Time Crusader recreational trailers because the Federal placard incorrectly lists axle capacity as 7,000 lbs instead of 6,000 lbs, which could lead to overloading.
Nissan is recalling 2017 Infiniti QX30 vehicles because the driver-side curtain air bag may fail to deploy in a crash, increasing injury risk.
Hyundai is recalling 2017 Santa Fe Sport vehicles because the tire pressure monitoring system may not warn drivers of underinflated tires, increasing crash risk.
Nissan is recalling 54,751 2012 Versa vehicles because degraded side impact sensor connector pins may cause air bags to deploy unexpectedly if a door is slammed.
REV Recreation Group is recalling specific 2015-2017 American Coach and Holiday Rambler motorhomes because interior step supports may be inadequately secured, creating an injury risk.
Kids II is recalling Oball Rattles because the plastic disc can break, releasing small beads that pose a choking hazard to young children.
Subaru is recalling 2017 Impreza vehicles because a software problem may cause the rearview camera display to malfunction, increasing crash risk.
Porsche is recalling 2016-2017 911 and 718 models because the passenger air bag inflator may fail to ignite, increasing injury risk in a crash.
One World Technologies is recalling Ryobi 8amp Electric Jet Fan Blowers because the internal plastic fan can break, discharging blades that pose a laceration hazard.
Goodman is recalling approximately 210,000 air handler units because the pull-out disconnects may fail to disable power, posing an electrical shock hazard to individuals servicing the equipment.
Volkswagen is recalling 2017 Beetle and Jetta GLI vehicles because incorrect tire information labels may cause operators to overload the vehicle, increasing crash risk.
Terumo is recalling Sarns Centrifugal Pumps because cracks in the housing can cause fluid leaks during cardiac procedures. No patient injuries have been reported.
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Biomet is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Tosoh Bioscience is recalling 682 HLC-723G8 analyzers because they may report inaccurate HbA1c values for patients with specific hemoglobin variants.
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Pier 1 Imports is recalling about 363,000 glass knobs sold in the U.S. because they can break and cause lacerations.
Archer Daniels Midland is recalling one lot of dry roasted almonds because they may contain undeclared cashews. The product was distributed in California.
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Riviana International is recalling Mahatma Saffron Yellow seasonings and long grain rice mixes due to the presence of foreign metal material.
Arrow International Inc is recalling 215,703 vascular catheter introduction kits nationwide because complaints were received regarding peel away sheaths flaring.
Biomet U.K., Ltd. is recalling Oxford Knee System Tibial Resector Body Tubes and Guides due to potential alumina inclusions that could cause the instruments to crack or separate.
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Falafel King is recalling 1,380 containers of Tzatziki Sauce due to undeclared milk on the label. The product was distributed in Colorado, New Mexico, Utah, and Nebraska.