State

New Jersey product recalls

73,190 recalls have nationwide distribution and so reach New Jersey. 9,768 additional recalls listed New Jersey specifically in their distribution scope.

What the numbers show

Total: 9,768
Critical: 1,249
Severe: 2,486
Most recent: 2026-09-30

Of the 9,768 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 2,486 (25%) are Severe.

Which agencies issued them

These figures cover only the 9,768 recalls whose distribution notice names New Jersey specifically. The 73,190 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

13201–13225 of 82958

ModerateFDA (Devices)·Z-1336-2024·2024-03-27
FDA Recalls Vascular Guidewire Introducer Due to Manufacturing Defect
Angiodynamics is recalling 959 units of MINI STICK MAX guidewire introducers due to voids in the sheath hub that may prevent proper guidewire placement. Users may experience procedure delays and need to exchange equipment.
Product
MINI STICK MAX 4F X 10 CM STIFF .018 SS/SS ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-751
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1338-2024·2024-03-27
Vascular Guidewire Introducer Sheath Recall Due to Manufacturing Defect
Angiodynamics is recalling certain MINI STICK MAX vascular guidewire introducer sheaths due to internal voids that may prevent guidewire passage during surgery, potentially causing procedural delays.
Product
MINI STICK MAX 5F X 10 CM STD .018 SS/SS ECHO 2.75" PG -Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-754
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1335-2024·2024-03-27
Angiodynamics Guidewire Introducer Devices Recalled for Manufacturing Defects
Angiodynamics recalls MINI STICK MAX guidewire introducer devices due to manufacturing defects in the internal lumen that may prevent guidewire passage and delay surgical procedures.
Product
MINI STICK MAX 4F X 10 CM STD .018 NI/TU ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-750
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1346-2024·2024-03-27
Guidewire Introducer Sheath from Angiodynamics Recalled for Manufacturing Defect
Angiodynamics is recalling 65 units of its MINI STICK MAX guidewire introducer sheath due to manufacturing defects that may prevent guidewires from passing through during surgical procedures.
Product
MINI STICK MAX 5F X 10 CM STD .018 NI/TU ECHO 1.6" PG- Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-775
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1313-2024·2024-03-27
Steris Endo Cleaning Indicator Recalled Due to Temperature Excursion
Mckesson Medical-Surgical is recalling Steris Endo Cleaning Indicator VERIFY RESITEST devices due to temperature excursions that occurred on January 8, 2024. The temperature drop could cause the indicator to produce incorrect or delayed test results.
Product
Steris Corporation Endo Cleaning Indicator VERIFY" RESITEST"
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1311-2024·2024-03-27
Sekisui OSOM BVBLUE Bacterial Vaginosis Control Kit recalled due to temperature exposure
A Sekisui Diagnostics control kit for bacterial vaginosis testing was recalled after exposure to temperatures below the validated storage range for up to 60 minutes due to refrigerator mechanical failure.
Product
Sekisui Diagnostics Control Kit OSOM¿ BVBLUE¿ Bacterial Vaginosis
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1315-2024·2024-03-27
Laboratory Control Material Recalled Due to Temperature Storage Excursion
Abbott Point of Care Control i-STAT Level 3 control material (Lot 121164) is being recalled due to temperature excursions in storage that could affect test accuracy. Affected units were distributed in Arizona, Pennsylvania, and Texas.
Product
Abbott Point of Care Control Control i-STAT¿ Level 3 1.7 mL
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1328-2024·2024-03-27
Liquid Protein Calibrators recalled for reference material realignment correction
Randox Laboratories is recalling 1,764 units of Liquid Protein Calibrators used in immunoassays due to realignment of C3 and Haptoglobin to the correct reference material standard. Distribution was limited to seven U.S. states.
Product
Liquid Protein Calibrators. C3 and Haptoglobin liquid protein calibrators used with Randox IgA, IgG, and IgM assays that require sample predilution.
Category
Medical Device
Distribution
7 states
ModerateFDA (Devices)·Z-1339-2024·2024-03-27
Angiodynamics surgical guidewire recalled for manufacturing defect
Angiodynamics is recalling 5,176 units of MINI STICK MAX guidewires due to manufacturing voids that prevent passage through the introducer during surgery. Surgeons may need to exchange the sheath to complete procedures.
Product
MINI STICK MAX 5F X 10 CM STD .018 NI/TU ECHO 2.75" PG Catalog Number: 45-756
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1305-2024·2024-03-27
Conductive Adhesive Gel Recalled Due to Thickness and Discoloration Issues
Natus Neurology is recalling TENSIVE Conductive Adhesive Gel (Lot A0623009) after complaints of improper thickness, discoloration, and in one case, patient skin irritation following use.
Product
TENSIVE Conductive Adhesive Gel, REF 016-401600
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1306-2024·2024-03-27
Natus Sleep Supplies Recalled for Conductive Adhesive Gel Quality Defects
Natus Neurology is recalling Sleep Supplies Start Kits due to defective conductive adhesive gel supplied by Parker Laboratories. The gel is too thick, discolored, and caused patient irritation in at least one case.
Product
natus neurology, Sleep Supplies Start Kit with Single Use Supplies for Embla EX Series Amplifiers, REF 024252
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1344-2024·2024-03-27
Guidewire Introducer Sheath with Manufacturing Defect Recalled by Angiodynamics
Angiodynamics is recalling MINI STICK MAX guidewire introducer sheaths due to manufacturing defects that may prevent guidewire passage. The defect may cause procedural delays requiring equipment exchange during vascular interventions.
Product
MINI STICK MAX 5F X 10 CM STD .018 SS/SS NON-ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-767
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·24V230000·2024-03-25
Doosan Portable Generator Trailers Recalled for Brake Wiring Defect
Doosan is recalling 2015-2023 Portable Generator Trailers because the electric brake harness was incorrectly wired, potentially disabling brakes.
Product
DOOSAN PORTABLE POWER — DOOSAN PORTABLE POWER MOBILE GENERATOR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V225000·2024-03-24
Mercedes-Benz Recalls 2023 Sprinter Vans for Electrical Fire Risk
Daimler Vans USA is recalling 2023 Mercedes-Benz Sprinter vans because a 12-volt ground connection may overheat, increasing the risk of fire or loss of drive power.
Product
MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 1500, SPRINTER 3500, SPRINTER 2500, SPRINTER 4500
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V226000·2024-03-22
Ford Recalls 2023-2024 Transit Vehicles for Tire Contact Defect
Ford is recalling 2023-2024 Transit vehicles with the Trail package because tires may contact the wheel arch liner, risking tire damage and loss of control.
Product
FORD — FORD TRANSIT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V223000·2024-03-22
Ford Maverick and Bronco Sport tires may have been manufactured incorrectly
Ford is recalling certain 2023 Maverick and Bronco Sport vehicles because the tires may have been manufactured incorrectly, which may result in a loss of vehicle handling and control.
Product
FORD — FORD MAVERICK, BRONCO SPORT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V229000·2024-03-22
Audi Recalls E-Tron GT Models Due to High-Voltage Battery Fire Risk
Volkswagen Group of America is recalling 2022-2023 Audi E-Tron GT and RS E-Tron GT vehicles because a high-voltage battery short circuit could cause a fire.
Product
AUDI — AUDI E-TRON GT, RS E-TRON GT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V228000·2024-03-22
Audi e-tron GT high voltage battery modules may short circuit
Volkswagen is recalling certain 2022-2024 Audi RS e-tron GT and e-tron GT vehicles because the high-voltage battery may experience a short circuit within the battery modules.
Product
AUDI — AUDI E-TRON GT, RS E-TRON GT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V222000·2024-03-22
Reading Truck Equipment Recalls 2021-2024 Dump Trucks Due to Fire Risk
Reading Truck Equipment is recalling 2021-2024 dump body trucks because inadequate clearance may allow the hood to contact the main electrical fuse terminal, increasing the risk of a fire.
Product
READING TRUCK EQUIPMENT — READING TRUCK EQUIPMENT DUMP BODIED TRUCKS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24E028000·2024-03-22
Suburban Recalls Slide-In Ranges with Overheating LED Backlight Boards
Suburban is recalling certain Slide-In Range models because the LED backlight circuit board may overheat, increasing the risk of a fire.
Product
EQUIPMENT:APPLIANCE:OVEN/STOVE/COOKTOP recall
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·24V224000·2024-03-22
Mercedes-Benz Recalls 2024 E-Class Vehicles for Wiring Harness Defect
Mercedes-Benz is recalling 2024 E350 and E450 vehicles because the transmission wiring harness may be routed too close to the driveshaft, potentially causing a loss of drive power.
Product
MERCEDES-BENZ — MERCEDES-BENZ E 350, E 450
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V227000·2024-03-22
Subaru Outback and Legacy occupant sensors may prevent airbag deployment
Subaru is recalling certain 2020-2022 Outback and Legacy vehicles because an Occupant Detection System capacitor may crack and short circuit, preventing front passenger airbag deployment.
Product
SUBARU — SUBARU LEGACY, OUTBACK
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V220000·2024-03-22
Ford Mustang low pressure fuel supply lines may be damaged or cut
Ford is recalling certain 2024 Mustang vehicles with 2.3L engines because the low-pressure fuel supply line may be damaged or cut, which can result in a fuel leak.
Product
FORD — FORD MUSTANG
Category
Vehicle
Distribution
Distributed nationwide
CriticalCPSC·24169·2024-03-21
Happiness USA Roller Ball Candy Recalled Due to Choking Hazard
Twenty Four Six Foods LLC is recalling all flavors of Happiness USA Liquid Rolling Candy because the rolling ball applicator can dislodge into a child's mouth, posing a choking hazard and risk of death.
Product
Happiness USA Liquid Rolling Candy
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·24171·2024-03-21
Starbucks-branded metallic mugs recalled due to burn and laceration hazards
Nestlé USA recalls about 440,500 metallic mugs from 2023 holiday Starbucks gift sets sold at Target, Walmart, and military retailers. The mugs can overheat or break when microwaved or filled with extremely hot liquid, causing severe burns and cuts. 10 people have been injured in 12 reported incidents.
Product
Metallic Mugs included in 2023 Holiday Starbucks-branded Gift Sets
Category
Consumer Product
Distribution
Distributed nationwide