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.
Siemens Healthcare Diagnostics is recalling Advia Chemistry Assay: Lactate units because N-Acetylcysteine and Metamizole can cause falsely depressed results.
Siemens Healthcare Diagnostics is recalling Dimension Uric Acid assays because N-Acetylcysteine and Metamizole can cause falsely low results.
Gillig is recalling 34 2016 Low Floor vehicles because the driver's side window may block too much light, reducing visibility and increasing crash risk.
Daimler Trucks North America is recalling 2,275 FCCC motorhome chassis due to a throttle sensor issue that may prevent the engine brake from activating, increasing crash risk.
Salsa Dianne is recalling Lemon Pesto Sauce because the label declares parmesan cheese but fails to declare milk, a major allergen.
Mobility Works is recalling 2014-2015 Ford and Chevrolet vans equipped with specific Ricon wheelchair lifts due to a risk of platform separation and injury.
Greater Pittsburgh Community Food Bank is recalling specific cans of Imperial Choice Mandarin Oranges because they may leak or burst, risking contamination by pathogens.
Siemens Healthcare Diagnostics is recalling Advia Chemistry Assays because N-Acetylcysteine and Metamizole can cause falsely depressed results.
Siemens is recalling ADVIA Chemistry Glucose Oxidase Assays because N-Acetylcysteine and Metamizole can cause falsely depressed results.
Siemens Healthcare Diagnostics is recalling Direct HDL Cholesterol assays because N-Acetylcysteine and Metamizole can cause falsely depressed results.
Medtronic is recalling 145 Kangaroo Connect Enteral Feeding Pumps because occlusion alarms may fail to sound, posing a risk to patients in hospital settings.
Pacific Cycle is recalling about 129,000 infant bicycle helmets sold at Target because loose magnetic buckle parts pose choking and ingestion risks to young children.
Target is recalling clear acrylic Hanukkah menorahs because they can melt when candles are burning, posing a fire hazard. No injuries or property damage have been reported.
Chrysler is recalling 2013-2016 Fiat 500e vehicles because a power inverter module defect may cause the propulsion system to shut down, increasing crash risk.
Chrysler is recalling aftermarket Mopar canvas seat covers for 2012-2016 RAM trucks because they can impede airbag deployment, increasing injury risk in a crash.
Chrysler is recalling 2016 Dodge Grand Caravan and Town and Country minivans because third row seatback nuts may be loose, posing an injury risk.
Supreme Corporation is recalling 2007-2009 Silver Crown and Ponyxpress vehicles because a bolt on the electric entry steps may fracture, causing the steps to become unstable.
Supreme is recalling 2010-2016 Classic American Trolley vehicles because missing welds on seat brackets may allow seat belt anchors to separate, increasing injury risk in a crash.
E-One is recalling 140 model year 2015-2016 Cyclone II, Quest II, and Typhoon emergency vehicles because pump intake strainers may be improperly soldered.
Hobby Lobby is recalling Little Wishes plush pacifier holders because parts can detach and pose a choking hazard to infants.
Hobby Lobby is recalling Little Wishes Chenille Stuffed Rattles because seams can separate, exposing stuffing and posing a choking hazard to infants.
Kovatch Mobile Equipment is recalling certain 2016-2017 emergency vehicles because pump intake strainers may be improperly soldered, potentially causing pump damage and reduced firefighting effectiveness.
Supreme Corporation is recalling 2011-2014 Signature Van, Iner-City, and Kold King vehicles because roof marker lights may short circuit and cause the corner caps to catch fire.
CareFusion 303, Inc. is recalling 23,397 Alaris PC units, Model 8015, because a super capacitor failure may cause a system error code at power-up.
Applied Medical Technology Inc is recalling Wilson Penile Implantation System Retractor Frames due to a reported open pouch that breaches sterilization validation.