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.
Philips is recalling 1,880 HeartStart MRx lithium-ion batteries because a defective component may prevent the battery from charging or delivering power to the monitor/defibrillator.
GNC is recalling Women's Iron Complete supplements because the blister packaging is not child-resistant, posing a risk of poisoning to children.
St. Jude Medical is recalling Deep Brain Stimulation leads where the most proximal unsegmented electrode may be made of MP35N instead of the required 90/10 platinum-iridium.
4Patriots, LLC is recalling Chicken a la King pouches because milk is not declared on the label. The product was sold nationwide in emergency kits.
Porsche is recalling 2017-2018 Panamera vehicles because a software failure may cause intermittent loss of electric power steering assist, increasing crash risk.
GE Healthcare is recalling 103 LOGIQ E10 Ultrasound Systems because a trans-esophageal probe may overheat, posing a risk of burn injury to patients.
Seagrave is recalling 2017-2018 Capital and Marauder II emergency vehicles because Whelen accessory brake lights may falsely illuminate, increasing crash risk.
CAO Group, Inc. is recalling fas.TRACT Coagulative Hemostatic Gel kits due to current Good Manufacturing Practice (cGMP) violations identified during a recent inspection.
Tosoh Bioscience is recalling AIA-900 and AIA-2000 analyzers due to a potential incubator slippage issue that may cause system errors and delays in patient test results.
Philips is recalling IntelliVue MX40 patient monitors because the speaker volume may be diminished or inaudible at altitudes above 4,500 feet.
Tosoh Bioscience is recalling 258 AIA-900 Automated Immunoassay Analyzers because internal harnesses may wear prematurely, causing the device to stop functioning and delaying patient test results.
Tosoh Bioscience is recalling AIA-2000 and AIA-900 analyzers because a timing belt issue can cause incubator slippage, leading to system errors and delays in patient test results.
CAO Group, Inc. is recalling SHEER DesenZ Desensitizing Treatment because cGMP violations were noted during the firm's most recent inspection.
CAO Group, Inc. is recalling BeeGentle Honey Flavored Topical Anesthetic because of current Good Manufacturing Practice (cGMP) violations found during a recent FDA inspection.
CAO Group, Inc. is recalling FastStat Topical Hemostat Introductory Kits because cGMP violations were noted during the firm's most recent inspection.
LGM Pharma LLC is recalling 1,307 kg of Thyroid Powder, USP, because the product has inconsistent levels of active ingredients levothyroxine and liothyronine.
COVIDIEN LLC is voluntarily recalling 1,522 Salem Sump Dual Lumen Stomach Tubes because one lot of 10 Fr tubes was incorrectly packaged in 16 Fr pouches.
Tosoh Bioscience is recalling Hemoglobin A1c Control material due to potential degradation that may cause testing delays.
Ford is recalling 410,289 F-Series trucks because water in the block heater cable can cause corrosion and a fire.
Eldorado is recalling 2017-2018 Arrivo, Passport, and E-Z Rider Max BRT buses because back seat cushions may not stay locked in place during a crash.
TerraTrike is recalling about 450 Rambler E.V.O. adult tricycles because the torque sensor can activate unexpectedly, causing the trike to power forward and posing crash and injury hazards.
TAP Worldwide is recalling Poison Spyder Customs-brand Tire Carriers that may lack required brake lights or disable rear cameras, increasing crash risk.
The Children's Place is recalling about 14,900 infant snowsuits because metal snaps can detach, posing a choking hazard to young children.
Triple E is recalling 2019 Serenity recreational vehicles because a metal cable may contact the battery terminal, creating a fire hazard.
Volkswagen is recalling 2018 Audi A5 Sportback vehicles because front suspension fasteners may not be sufficiently tightened, which could cause a front wheel to become loose.