State
73,817 recalls have nationwide distribution and so reach New Jersey. 9,782 additional recalls listed New Jersey specifically in their distribution scope.
Of the 9,782 recalls naming New Jersey we have scored against our rubric, 1,246 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,944 (30%) are Severe.
Which agencies issued them
These figures cover only the 9,782 recalls whose distribution notice names New Jersey specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Edwards Lifesciences is recalling one SAPIEN 3 Transcatheter Heart Valve because it was packaged with the incorrect valve size relative to the label.
Cardinal Health is recalling 8,928 Presource PBDS kits because a defect in the Gatorade pouch seal caused the pouch to leak within the kit.
The Hain Celestial Group is recalling alba BOTANICA sport mineral sunscreen because the wrong product formulation was placed in the packages.
Philips is recalling 32 Ingenuity Digital PET/CT Systems because a block connecting the patient pallet to the couch may be assembled incorrectly, potentially causing a misaligned screw.
Cardinal Health is recalling Presource PBDS kits because a defect in the Gatorade pouch seal caused the pouch to leak within the kit.
Stryker is recalling 180 reprocessed Harmonic Ace shears because they may display an error code preventing use.
Siemens Healthcare Diagnostics is recalling 1,446 units of Dimension Vista CTNI Sample Diluent because a defective cap septum may cause erroneously elevated test results.
Valeris Medical is recalling 113 Apollo XT Suture Anchors because the labels incorrectly identified the material as titanium instead of PEEK.
Fx Solutions is recalling specific proton beam therapy heads due to a breach in the external blister packaging.
Cardinal Health is recalling 8,928 Presource PBDS kits because a defect in the Gatorade pouch seal caused the pouch to leak within the kit.
Fx Solutions is recalling specific lots of Humelock Offset Heads due to a breach in the external blister packaging.
Intel-GE Care Innovations LLC is recalling the Health Harmony Mobile application because patient data sometimes failed to sync with the backend database in a timely manner.
Siemens is recalling 1,195 units of Dimension Vista MULTI 2 SDIL diluent because a defective septum may cause erroneously elevated test results.
Cardinal Health is recalling 8,928 Presource PBDS kits because a defect in the Gatorade pouch seal caused the pouch to leak within the kit.
SynTec is recalling S3B 45-inch Restraint School Bus Seats because the mounting foot may pull through the bolted joint at the bus floor, increasing injury risk in a crash.
JCPenney is recalling Okie Dokie Denim Patches Shortie shorts because the patches can detach, posing a choking hazard to young children.
Ross Stores is recalling Bronze Hammered bistro chairs because the frames can break, posing a fall hazard. Consumers should stop using the chairs and return them for a full refund.
Karma Automotive is recalling 2018 Revero vehicles because the driver's side exterior rearview mirror may use convex glass instead of flat glass, failing federal safety standards.
Meritor is recalling specific wheel studs installed in steer axle hubs because improper heat treatment may cause them to fail, potentially leading to wheel detachment.
Jost International is recalling certain Outboard Sliders because a narrow bracket may allow the trailer to separate from the tractor, increasing crash risk.
Braun Corporation is recalling 2012-2018 BraunAbility Dodge and Chrysler wheelchair vans because brake lines may be disconnected, reducing electronic stability control performance.
Daimler Trucks is recalling 2018-2019 Freightliner Business Class M2 trucks because an incorrectly installed steering shaft may disconnect the steering wheel from the front wheels.
Van-Con is recalling 2011-2018 33803 Dual Rear Wheel school buses because seat foam may not absorb enough impact in a crash, increasing injury risk.
The USDA FSIS issued a public health alert for Hungry Man frozen dinners containing whey powder recalled due to possible Salmonella contamination. No adverse reactions have been reported.
Daimler Trucks is recalling 2017-2019 Freightliner Cascadia trucks because the instrument cluster may fail to check ABS and ESC warning lights, increasing crash risk.