State
73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Jaguar Land Rover is recalling 2018 Range Rover Evoque convertibles with 20-inch wheels because the tire pressure monitoring system may fail to warn drivers of low pressure.
CPSC recalls Greenworks, Kobalt, and Snapper cordless electric chainsaws because the chain brake guard can fail, allowing the saw to continue operating and posing an injury hazard.
Alstyle is recalling infant bodysuits because crotch snaps can detach, posing a choking hazard to young children. No injuries have been reported.
Hunter Douglas is recalling Luminette privacy sheer blinds because the cord restraints can break, posing a strangulation hazard to children.
John Deere is recalling about 3,700 ZTrak riding mowers because the blades can rotate while the operator is off the seat, posing a laceration risk.
BotanicalNow is recalling BodySlim Herbal capsules because FDA analysis found undeclared sibutramine, a substance not approved for use in this product.
Vyaire Medical is recalling 16,670 Infant AirLife single-limb circuits and humidification chambers because a manufacturing error may cause water to back up into the patient's airway.
Vornado Air is recalling Sunny CS nursery space heaters because a broken motor mount can cause the heating element to ignite, posing fire and burn risks.
Vyaire Medical is recalling 16,670 Infant AirLife humidification chambers because a manufacturing error may cause water to overflow into the patient's airway.
International Laboratories, Inc. is recalling Pravastatin Sodium Tablets 10 mg because bottles may contain 20 mg tablets.
Vyaire Medical is recalling 16,670 units of Adult Air-Life single-limb circuits with Humidification Chambers due to a manufacturing error that may cause water overflow into patient airways.
Sun Pharmaceutical Industries is recalling 393 vials of Doxorubicin Hydrochloride Liposome Injection due to a lack of assurance of sterility.
Toyota is recalling 48,672 vehicles because air bag sensors may fail, preventing deployment in a crash and increasing injury risk.
International Laboratories, Inc. is recalling Pravastatin Sodium Tablets, 20 mg, because bottles may contain 10 mg tablets. Patients should contact their healthcare provider.
Nissan is recalling 2015-2017 Juke Nismo RS vehicles because brake fluid may leak into the brake booster, reducing brake performance and increasing crash risk.
Vyaire Medical is recalling 16,670 AirLife Humidification Chambers and circuits because a manufacturing error may cause water to back up into patient airways.
Philips is recalling Brilliance iCT CT systems due to software issues affecting scan functions and safety features.
John Deere is recalling about 600 model 2025R compact utility tractors because the brakes can fail, posing crash and injury hazards.
Siemens is recalling 36 units of Syngo Imaging version V31 software due to a potential risk of data loss relevant to diagnosis.
DLC Laboratories is recalling Earth's Care Eczema Lotion due to microbial contamination. The product was distributed nationwide.
LEDVANCE is recalling SYLVANIA recessed canister light kits because they can short circuit, posing a shock and electrocution hazard.
Triumph is recalling 2016-2018 Thruxton motorcycles because the engine may stall during rapid throttle changes, increasing crash risk.
Philips Medical Systems is recalling 559 Brilliance iCT CT systems due to software issues affecting scan functions and safety features.
Marksans Pharma Inc. is recalling 4,127,500 ibuprofen tablets due to odor complaints and CGMP deficiencies. The product was distributed nationwide to repackaging firms.
Odan Laboratories is recalling 179 kits of Dry to Normal Skin Starter Kit because the product failed stability specifications at 12 months.