State
72,986 recalls have nationwide distribution and so reach New Jersey. 9,761 additional recalls listed New Jersey specifically in their distribution scope.
Of the 9,761 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 2,484 (25%) are Severe.
Which agencies issued them
These figures cover only the 9,761 recalls whose distribution notice names New Jersey specifically. The 72,986 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Sysco Corporation is recalling egg salad sandwiches (HKSAN169, 1/5.76 oz) because cucumbers used in the product may be contaminated with Salmonella.
Philips is recalling certain Intera Achieva 1.5T Pulsar MRI systems due to a potential component failure in the gradient coil that could generate smoke and/or fire, risking patient and operator injury or death.
About 100,000 Crayan Mattresses fail to meet federal flame-resistance standards, posing a fire hazard. Consumers should stop using them immediately and contact Crayan for a refund.
Olympus Corporation of the Americas is recalling Soltive Reusable Laser Fibers due to risk of thermal incidents including smoke, sparks, burning, or unsteady flames during surgery, caused by fiber fracturing.
Sysco Corporation is recalling multiple fresh salad products because cucumbers used in the products have the potential to be contaminated with Salmonella. The recall affects salads sold under brands including East Coast Fresh and Created Fresh.
Sysco Corporation is recalling Created Fresh Southwest Breakfast Bowl units because cucumbers in the product have the potential to be contaminated with Salmonella.
Chrysler is recalling Mopar Center Stack Displays with a software error that may prevent the rearview camera image from displaying, increasing crash risk.
Tesla is recalling certain 2026 Model Y and Model 3 vehicles because seat back fasteners may have been improperly tightened, potentially affecting proper occupant restraint during a crash.
Mazda is recalling 2025 CX-50 Hybrid vehicles because the gear shifter can move to Drive without pressing the brake pedal, increasing crash risk.
Polaris is recalling Model Year 2023-2024 Ranger XP Kinetic and Model Year 2025 Pro XD Kinetic ROVs because water can leak through a cracked filter into the high-voltage charging harness and cause a fire. The company has received 47 reports of filter failures, including six reports of melting or fire.
YaFiti 12-Drawer White Dressers pose serious tip-over and entrapment hazards to children if not anchored to the wall, violating federal standards. About 6,000 units sold on Amazon from September 2023 through March 2025.
Olympus Corporation of the Americas is recalling the SOLTIVE Pro SuperPulsed Laser System due to risk of unexpected smoke, sparks, burning, or unsteady flames caused by fiber fracturing during clinical use.
R&M Refresher brand Instant Milk Tea Brown Sugar Flavor is recalled because the ingredients contain milk (Whey Powder, Sodium Caseinate) but the label does not declare milk as an allergen.
MicroAire Surgical Instruments is recalling the SmartRelease ESTR Onyx Blade Assembly due to a potential risk that the blade can unintentionally cut tissue before the user deploys it.
R&M Trading LLC is recalling Instant Milk Tea Original Flavor because the label does not declare milk, despite containing whey powder and sodium caseinate, which are milk-derived ingredients.
Microbiologics Inc is recalling KWIK-STICK quality control kits because products were packaged with incorrect microorganism swabs, which may lead to delayed diagnosis of patient samples in clinical laboratories.
Mobius Mobility LLC is recalling 442 units of the iBOT PMD (Personal Mobility Device) with software version 01.05.24 due to a software issue that could cause the device to tip over during Balance Mode operation.
BD TEXIUM Closed Male Luer devices may leak at the interface between the closed male luer component and needle-free connector. The leak could cause procedure delays, treatment interruptions, exposure to hazardous drugs, and underdosing of medication.
Tecfen Medical is recalling its 15 degree Stab Knife (Model QKN1501) due to sterility assurance concerns. The ophthalmic knife is used in eye surgeries and was distributed in the US and internationally.
Belmont Instrument's Allon 2001 device may heat water above safe limits if sensor connections fail and temperature alarms are disabled. The patient wrap may exceed its set temperature without user notification.
REV is recalling 2025-2026 Fleetwood Altitude and Holiday Rambler Incline motorhomes because water intrusion may cause electrical components to fail, potentially disabling carbon monoxide or propane detectors.
Tecfen Medical is recalling its 2.2mm Slit Knife (Model QKN2261) due to sterility assurance concerns. The ophthalmic knife is used to create precise incisions for eye surgery.
GE Medical Systems is recalling MUSE 5 Systems due to a vulnerability that could allow unauthorized access to patient data. The MUSE Administrator Account credentials could potentially be used to log into affected systems from the local network and manipulate recorded cardiovascular patient data.
Contamac Nutrifill Physiologic formula contact lens insertion solution is being recalled because it may lack sterility. The affected product was distributed nationwide.
Tecfen Medical is recalling 2.0mm Crescent Knife ophthalmic surgical instruments (Model QKN1010, Lot ZGY24071501-03) due to sterility assurance concerns. The affected devices were distributed in the US and internationally.