State
73,737 recalls have nationwide distribution and so reach New Jersey. 9,780 additional recalls listed New Jersey specifically in their distribution scope.
Of the 9,780 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 2,942 (30%) are Severe.
Which agencies issued them
These figures cover only the 9,780 recalls whose distribution notice names New Jersey specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Huffy is recalling Torex 24V ride-on toy UTVs sold at Walmart because the toys can unexpectedly move when the battery is connected, posing an injury hazard.
Coloplast is recalling 8,962 Titan Pump units due to a potential increased occurrence of pump fracture over the device's lifetime.
RaySearch Laboratories is recalling RayStation software because missing data may cause treatment plans to reference incorrect regions or points of interest.
Mevion Medical Systems is recalling eight MEVION S250 and S250i proton radiation treatment systems because treatment beam information may disappear from the console screen while the beam continues to deliver.
Intuitive Surgical is recalling 454 ION Fully Articulating Catheters because the distal tip ring may become dislodged during use.
ViewRay is recalling three MRIdian systems because receive coil components may reach elevated temperatures, posing a potential risk of burn injury to patients or users.
Jubilant Cadista Pharmaceuticals is recalling 4,416 bottles of clomipramine hydrochloride capsules because they failed tablet/capsule specifications.
Medtronic is recalling 37 units of the Cardioblate CryoFlex Surgical Ablation Probe due to potential defects in the sterile barrier pouch seals.
Medtronic is recalling 3 units of Cardioblate CryoFlex Surgical Ablation Probes because of a potential defect in the sterile barrier pouch seals.
Medtronic is recalling 57 units of the Cardioblate CryoFlex Surgical Ablation Probe due to a potential defect in the sterile barrier pouch seals.
Teligent Pharma is recalling one lot of Triamcinolone Acetonide Lotion because it does not meet assay results.
Luminex is recalling 2,838 Verigene Processor SP units because field service engineers used unapproved test fixtures to calibrate the devices.
Advanced Bionics is recalling 53 PowerCel 230 batteries for cochlear implants because they may be mislabeled with incorrect battery life information.
Heritage Pharmaceuticals is recalling specific bottles of Felodipine Extended Release Tablets because routine testing found out-of-specification impurities.
Fresenius Kabi is recalling Doxorubicin Hydrochloride Injection vials because testing found trace amounts of octreotide.
Medtronic is recalling 15 units of the Cardioblate CryoFlex Surgical Ablation Probe due to a potential defect in the sterile barrier pouch seals.
Fusion Health and Vitality LLC is recalling 5,000 bottles of Immune Boost because the product was marketed with drug claims without an approved NDA or ANDA.
Luminex is recalling 2,838 Verigene Processor SP units because field service engineers used unapproved test fixtures to calibrate and verify the devices.
Advanced Bionics is recalling 28 AB PowerCel 170 batteries due to mislabeling that may indicate incorrect battery life.
Hyundai is recalling 2019-2021 Kona Electric and 2019-2020 Nexo vehicles because a software issue may reduce braking performance, increasing crash risk.
Vac-Tron is recalling specific excavator trailers because they lack required rear impact guards, increasing the risk of injury if struck from behind.
Hyundai is recalling specific 2011-2016 models because engine connecting rod bearings may wear prematurely, potentially causing engine damage, fire, or stalling.
Forest River is recalling 2021 Coachmen Galleria motorhomes because damaged brake hoses may leak fluid, increasing crash risk.
Nissan is recalling 2002-2006 Sentra vehicles because passenger air bag inflators may explode in a crash, posing a risk of serious injury or death.
Halcore is recalling 2020 Horton Type I and III emergency vehicles because a display processor may stop working, potentially delaying emergency services.