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.
Baxter Healthcare is recalling HomeChoice and HomeChoice Pro automated peritoneal dialysis cyclers because the keypad buttons may activate without being pressed.
Sunrise Medical is recalling six Quickie Q7 Adult Rigid Wheelchairs because the height-adjustable handle may dislodge due to failing locking mechanisms.
Gibbs Sports Amphibians is recalling about 320 Quadski and Quadski XL amphibious vehicles because the handlebar can fail, causing loss of control and injury risk.
Terex is recalling 2013 Hi-Ranger trucks because a bearing installation issue may allow the platform to rotate without operator control, increasing injury risk.
Blue Bird is recalling 2011-2016 All American school buses because exhaust hangers may fail, causing components to fall onto the roadway.
Performance Packaging is recalling PouchPop toppers because the tube can separate from the base, posing a choking hazard to young children.
Blue Bird is recalling 2011-2016 All American rear engine transit buses because exhaust system hangers may fail, potentially causing housings to fall onto the roadway.
Mack is recalling 2015 LEU trucks because a short door component may prevent opening from inside, hindering emergency egress.
Brammo is recalling 2013-2014 Empulse and Empulse R motorcycles because oil may leak from the transmission onto the rear tire, increasing crash risk.
Ford is recalling 2014 Transit Connect vehicles because upper seat belt bolts may be improperly torqued, posing an injury risk in crashes.
All Wheel Drive Equipment Mfg. is recalling one 2011 Ford F-550 truck because a PTO pressure switch may leak oil onto the exhaust, increasing fire risk.
Sunbeam is recalling Holmes oil-filled heaters because they can spray heated oil, posing a scald hazard. No injuries have been reported.
Dick's Sporting Goods is recalling Fitness Gear Inversion Tables because customers reported falling and sustaining injuries. The products were distributed nationwide.
Vosges Haut-Chocolat is recalling Festival of Lights Chanukkah Gift Box Sets because the plastic menorah can catch fire if candles burn to the base.
American Roland Food Corp. is recalling Roland brand Bruschetta, Italian-Style Appetizer, because glass fragments were found in the product.
Honda is recalling 2003-2004 Odyssey and 2003 Acura MDX vehicles because electrical noise may cause air bags to deploy unexpectedly, increasing injury risk.
Maquet Medical Systems USA is recalling six units of the Tegris System because a software error switches leg movement commands for the Magnus OR table.
Quest Nutrition is recalling specific lots of QuestBar protein bars due to the possibility of plastic pieces introduced by an ingredients supplier.
Siemens is recalling 11 Ysio Max, Luminos dRF Max, and Agile Max systems because software errors may cause images to flip, leading to incorrect labels and potential misdiagnosis.
Chrysler is recalling 2014-2015 Jeep Cherokee vehicles because side and seat air bags may deploy unexpectedly, increasing the risk of injury or a crash.
Ford is recalling 2010-2013 Taurus and 2011-2013 Lincoln MKS vehicles because an interior door handle spring may unseat, preventing the handle from returning to its stowed position.
BD Biosciences is recalling one lot of CD8 PE reagent contaminated with CD4 FITC, which may cause incorrect patient data.
Cordis Corporation is recalling one unsterilized unit of the POWERFLEX PRO PTA Dilatation Catheter from a demonstration lot left at a hospital.
Ferno-Washington Inc is recalling 46 Model 35X stretchers because wheel castor assemblies may loosen, posing a risk of injury.
Jaguar is recalling 2012-2015 XK vehicles because front side lamps may turn off after five minutes, reducing visibility and increasing crash risk.