State
73,388 recalls have nationwide distribution and so reach New Jersey. 9,769 additional recalls listed New Jersey specifically in their distribution scope.
Of the 9,769 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 2,939 (30%) are Severe.
Which agencies issued them
These figures cover only the 9,769 recalls whose distribution notice names New Jersey specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Certain 2022 RAM 1500 vehicles have front seat belt retractors with improperly welded components that may fail to restrain occupants during a crash. Chrysler is replacing the affected retractors free of charge.
Ekouaer children's bathrobes fail to meet federal flammability standards for sleepwear, posing a burn risk to children. About 9,200 units sold on Amazon between March 2020 and July 2021 are affected.
Chrysler is recalling specific Mopar 3.0L Diesel Engines because the high-pressure fuel pump may fail, causing the engine to stall and increasing crash risk.
Newair is recalling about 11,750 Magic Chef Air Fryers because they can overheat, posing fire and burn hazards. Consumers should stop using them immediately and contact Newair for a refund.
Fresenius Kabi is recalling the Ivenix Infusion System (IIS) LVP Software version 5.2.0 because the display screen may freeze and become unresponsive, stopping medication flow and requiring immediate clinician intervention.
Philips Respironics is recalling 930,813 DreamWisp Nasal Masks worldwide due to missing warnings about magnetic components that could interfere with implantable medical devices or cause metallic splinters.
Philips Respironics is recalling DreamWear Full Face CPAP masks due to missing warnings about magnetic components that may pose risks to patients with implantable devices or metallic eye splinters.
Daimler Trucks North America is recalling 2011-2023 Thomas Built EFX and HDX school buses because exterior roof panels may separate during a crash.
Kenover Marketing Corp. is recalling Mighty Sesame Organic Tahini over potential Salmonella contamination. Approximately 13,766 units were distributed to stores across 20 states.
Philips Respironics Amara View Full-Face Mask lacks critical safety warnings about magnetic components for patients with implantable medical devices. The Class I recall affects 5.6 million units worldwide.
Philips Respironics is recalling the Therapy Mask 3100 NC/SP because the product lacks warnings about magnetic components that may affect patients with implantable devices or metallic splinters in the eyes.
Philips Respironics is recalling Wisp and Wisp Youth nasal masks because they lack warnings about magnetic components that could interfere with implanted medical devices or cause eye injuries from metallic splinters.
Cipla recalls Arformoterol Tartrate Inhalation Solution due to environmental monitoring failure affecting sterility assurance.
IN MY BATHROOM LLC is recalling 485 units of the Seago SG-153 handheld UV-C germicidal wand nationwide due to excessive ultraviolet-C radiation. Consumers should stop using the device and contact the manufacturer for instructions.
Zimmer, Inc. is recalling certain G7 Acetabular System acetabular shells (52 MM and 60 MM) because the outer sterile package has corner walls thinner than specification, which could crack during transit and potentially lead to surgical complications or infection.
Wright Medical Technology recalls 32 units of Stryker EVOLVE Proline Stem due to labeling mismatch: outer packages are labeled with one stem size but contain a different size. Surgeons should verify device size before implantation.
Blue Bird is recalling 2023 Vision and All-American transit buses because the entrance door handrail diameter is too small to meet ADA standards, posing a slip and fall risk.
Wright Medical is recalling EVOLVE Proline Stem devices due to labeling errors where the outer package does not match the device inside. Affected devices are size-mismatched, which could lead to incorrect surgical placement.
Hologic recalls 233 BioZorb LP Markers nationwide due to removable labels showing incorrect expiration dates. Implants labeled with January 2022 dates may be mistakenly used after their actual July 2024 expiration.
WFM 365 Organic Creamy Caesar dressing is recalled because the product does not declare wheat and soy allergens on its label. Consumers with wheat or soy allergies should not consume this product.
Synthes is recalling Hammertoe Continuous Compression Implant (CCI) Kits because the drill pin is incompatible with the included drill template, which may delay surgery or cause soft tissue damage and adverse tissue reactions.
2022 Volkswagen ID.4 vehicles have rearview cameras that may be delayed or deactivated, reducing rear visibility and increasing the risk of crashes. Dealers will provide a free software update.
Philips has recalled MR Patient Care Portal 5000 desktop units (Model 453564792561) due to intermittent audio failure. The device may fail to produce audio, and standard troubleshooting does not reliably resolve the issue.
Dr. Reddy's Laboratories is recalling Phytonadione Injectable Emulsion USP due to out-of-specification aluminum content results found during 12-month stability testing.
AuroMedics Pharma LLC is recalling one lot of Tranexamic Acid Injection due to the presence of metal particles found in a vial. The affected product was distributed nationwide.