State
73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Greenfield World Trade is recalling Excalibur EZ DRY food dehydrators because they can overheat, posing a fire hazard and causing minor burn injuries.
Suzuki is recalling 2010-2013 Kizashi vehicles because the front passenger air bag may deactivate if the system misclassifies an adult as a child.
FIRMAN Power Equipment is recalling P03615 portable generators sold at Costco because the carbon canister can leak gas, posing a fire hazard.
Yamaha is recalling 198 2019 YZFR3 motorcycles because porosities in the front brake lever may cause it to break under strong force, increasing crash risk.
Edwards Lifesciences is recalling Fogarty Dilation Atrioseptostomy Catheters due to reports of balloon fragmentation or detachment and difficulty deflating the balloon after deployment.
Edwards Lifesciences is recalling Miller Balloon Atrioseptostomy Catheters due to difficulty deflating the balloon and reports of fragmentation or detachment.
COVIDIEN LLC is recalling 7,248 units of the Endo Clinch II Auto Suture Grasper because the sterilization method used was not consistent with the labeling and approved method.
Guangzhou Improve Medical Instruments is recalling 550,000 Prevent G Safety Winged Blood Collection Sets because the hub needle detached during use.
Fresenius Kabi is recalling 342 CATSmart autotransfusion devices because tubing may contact the washing chamber, causing wear or puncture.
Patagonia Provisions is recalling Chipotle Lime Savory Seeds labeled as gluten-free because they contain gluten in excess of 20 ppm.
Brainlab AG is recalling specific versions of RT Elements software due to a potential for incorrect dose distribution calculations when using the Pencil Beam algorithm on the GPU.
Mineralife LLC is recalling Trace Minerals Dietary Supplement bottles due to potential contamination with Pseudomonas aeruginosa.
DAVIDsTEA is recalling about 700 Valentine's Day stackable mugs because they were mislabeled as microwave safe, posing a fire hazard if used in a microwave.
Siemens Medical Solutions USA is recalling 120 digital linear accelerators nationwide to prevent patient or user injury from disabling the Automatic Motion Protection function.
Indian Motorcycle is recalling 2014 Chief and Chieftain models because a Vehicle Control Module issue may cause all front lights to go out, increasing crash risk.
Starbucks is recalling Bodum co-branded coffee presses because the plunger knob can break and expose a metal rod, posing a laceration hazard.
Ortho-Clinical Diagnostics is recalling 80 VITROS XT 7600 Integrated Systems because a software error may cause incorrect test results without alerting the user.
Patagonia Provisions is recalling Savory Seeds Variety Packs labeled gluten-free because they contain gluten in excess of 20 ppm.
PACCAR is recalling 2020 Peterbilt and Kenworth trucks because mirror glass may detach, creating a road hazard and reducing driver visibility.
Thoratec Corp. is recalling HeartMate 3 Coring Tools because a small black plastic particle was observed in a patient's left ventricle during an implant procedure.
Arthrex, Inc. is recalling specific lots of Arthrex Oval Burr devices because they may generate excessive heat during use, posing a risk of injury to patients.
Stryker is recalling 355 Performance Series Sagittal Blades due to a potential breach in sterility caused by improper packaging positioning during manufacture.
Smiths Medical ASD Inc. is recalling specific lots of Jelco ViaValve safety intravenous catheters due to a V-shaped puncture at the base of the catheter.
Carestream Health is recalling 37 OnSight 3D Extremity Systems because a software error may leave companion imaging volumes in the original patient's exam during re-assignment.
Covidien LLC is recalling 148 procedure kits because the sterilization method used was not consistent with the labeling and approved method.