State
72,966 recalls have nationwide distribution and so reach New Jersey. 9,760 additional recalls listed New Jersey specifically in their distribution scope.
Of the 9,760 recalls naming New Jersey we have scored against our rubric, 1,249 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,483 (25%) are Severe.
Which agencies issued them
These figures cover only the 9,760 recalls whose distribution notice names New Jersey specifically. The 72,966 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Wartech is recalling 2022-2025 SpecialContainer trailers because an incorrect piping fitting may leak air, reducing brake pressure and increasing crash risk.
About 78,000 Lifepro Bioremedy infrared sauna blankets are being recalled after 65 reports of overheating, including 32 reports of burn injuries.
Ford is recalling certain 2021-2023 Bronco vehicles because the front seats may have a loose or dislodged seat frame height-adjust pivot bolt, so the seat may not restrain an occupant in a crash.
Chrysler is recalling certain 2018-2026 Ram ProMaster vehicles because the electrical circuit for the radiator fan may overheat, increasing the risk of a fire.
LEACHOI Bed Rails are being recalled because users can become entrapped within the rail or between the rail and the mattress, and the rails lack required hazard warning labels.
About 13,440 Scotch TL909-50 thermal laminators are being recalled because they may overheat, posing a burn hazard. No incidents have been reported.
About 1,500 Scepter B62 gas and oil combination fuel containers are being recalled because they lack flame mitigation devices and the spout is not child-resistant.
Maserati is recalling certain 2023-2025 Grecale, Granturismo and Grancabrio vehicles because the headlights may be missing adjustment prevention caps, allowing them to be improperly adjusted.
About 530 Pack-N-Stroll Premium Folding Utility Wagons sold at Costco are being recalled because a gap can entrap a child's head and the wagon has no restraint system.
About 410 Bealife 5-drawer dressers sold on Amazon are being recalled because they are unstable when not anchored to a wall and violate the STURDY Act standard.
About 840 Scepter B62 gas and oil combination fuel containers are being recalled because they lack flame mitigation devices and the spout is not child-resistant.
Olympus is recalling Bronchovideoscope BF-XT190 units for instructions-for-use updates on safe use with laser, argon plasma coagulation and high-frequency therapy equipment.
Olympus is recalling OES Bronchofiberscope BF Type MP60 units for instructions-for-use updates on safe use with laser, argon plasma coagulation and high-frequency therapy equipment.
Olympus is recalling Bronchovideoscope BF-H1100 units for instructions-for-use updates on safe use with laser, argon plasma coagulation and high-frequency therapy equipment.
Olympus is recalling OES Bronchofiberscope BF Type XT40 units for instructions-for-use updates on safe use with laser, argon plasma coagulation and high-frequency therapy equipment.
D & M Smoked Fish is recalling 2,022 pieces of Haifa Cold Smoked Salmon because the product is contaminated with Listeria monocytogenes.
D & M Smoked Fish is recalling 348 pieces of Haifa Cold Smoked Seabass because the product is contaminated with Listeria monocytogenes.
Olympus is recalling EVIS EXERA II Bronchovideoscope BF Type 1T180 units for instructions-for-use updates on safe use with laser, argon plasma coagulation and high-frequency therapy equipment.
IntegraDose Compounding Services is recalling 853 bags of Oxytocin 30 Units/500 mL in 0.9% sodium chloride after testing revealed there was no oxytocin in the IV bag.
Olympus is recalling Bronchovideoscope BF-Q170 units for instructions-for-use updates on safe use with laser, argon plasma coagulation and high-frequency therapy equipment.
Olympus is recalling EVIS EXERA Bronchovideoscope BF Type XT160 units for instructions-for-use updates on safe use with laser, argon plasma coagulation and high-frequency therapy equipment.
Cook Medical is recalling 695 Zenith Alpha 2 Thoracic Endovascular Grafts because affected devices may contain PTFE coating scrapings that could be released during deployment.
Olympus is recalling EVIS EXERA II Bronchovideoscope BF Type P180 units for instructions-for-use updates on safe use with laser, argon plasma coagulation and high-frequency therapy equipment.
Olympus is recalling EVIS EXERA II Bronchovideoscope BF Type 1TQ180 units for instructions-for-use updates on safe use with laser, argon plasma coagulation and high-frequency therapy equipment.
Olympus is recalling EVIS EXERA III Bronchovideoscope BF-Q190 units for instructions-for-use updates on safe use with laser, argon plasma coagulation and high-frequency therapy equipment.