State

New Jersey product recalls

73,100 recalls have nationwide distribution and so reach New Jersey. 9,767 additional recalls listed New Jersey specifically in their distribution scope.

What the numbers show

Total: 9,767
Critical: 1,249
Severe: 2,486
Most recent: 2026-09-25

Of the 9,767 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 9,767 recalls whose distribution notice names New Jersey specifically. The 73,100 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

10301–10325 of 82867

HighFDA (Food)·F-1828-2024·2024-10-02
Potato and Onion Vareniki Recalled Due to Undeclared Wheat
M&P Food Productions is recalling Potato & Onion Vareniki due to undeclared wheat. Consumers with wheat allergies or celiac disease should not consume this product.
Product
Potato & Onion Vareniki; M&P Food Production; NET WT. 14oz; HANDMADE; Keep Frozen; DOUGH INGREDIENTS: Flour, eggs, water, oil (soybean), salt; FILLING INGREDIENTS: Potato, Fried Onion; UPC: 707163026167
Category
Food
Distribution
7 states
HighFDA (Food)·F-1834-2024·2024-10-02
Imported Pickled Garlic Recalled for Undeclared Fish Allergen
Niitakaya USA Inc is recalling Miso Katsuo Ninniku pickled garlic because it contains undeclared fish allergen. Consumers with fish allergies should not consume this product.
Product
Miso Katsuo Ninniku (Pickled Garlic), Net WT 5.2 OZ (147g) Products of China; Imported By Niitakaya U.S.A. Inc., Motebello, CA 90640 ITEM No. 3701
Category
Food
Distribution
7 states
HighFDA (Food)·F-1825-2024·2024-10-02
M&P Delicacies Pirozhki Frozen Pies Recalled for Undeclared Wheat and Milk
M&P Delicacies frozen pirozhki pies contain undeclared wheat and milk allergens. Consumers with allergies to these ingredients should not consume the product.
Product
M&P Delicacies PIROZHKI (PIES) with POTATOES; INGREDIENTS: Flour, eggs, butter, vegetable oil, dry yeast, sugar, salt; Filling: Potatoe, onion, salt, pepper; 1 SERVING READY TO EAT; KEEP FROZEN
Category
Food
Distribution
7 states
ModerateFDA (Drugs)·D-0662-2024·2024-10-02
Sunscreen product recalled for microbial contamination nationwide
SHEET SPF 30 Mineral sunscreen is being recalled for microbial contamination. The product was distributed nationwide.
Product
SHEET SPF 30 MINERAL — SHEET SPF 30 MINERAL (TITANIUM DIOXIDE, ZINC OXIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3189-2024·2024-10-02
Stainless Steel Sims Uterine Sound Recalled for Incorrect Part Number
CooperSurgical, Inc. is recalling the Stainless Steel Sims Uterine Sound (Part Number 64-601) because some units were laser-marked with incorrect part numbers during manufacturing. No injuries have been reported.
Product
Stainless Steel Sims Uterine Sound, Part Number 64-601
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3210-2024·2024-10-02
AVS Anchor-C Cervical Cage Instructions for Use Labeling Correction
Stryker Spine recalled the electronic Instructions for Use revision 5 for the AVS Anchor-C Cervical Cage System because specific indications language for the US and Canada was inadvertently removed.
Product
AVS Anchor-C Cervical Cage System Instructions For Use (IFU)- eIFU (revision 5)-Indicated for anterior cervical interbody fusion procedures in skeletally mature patients with cervical disc disease at one level from the C2-C3 disc to the C7-T1 disc.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3254-2024·2024-10-02
Cook Biotech Recalls Biodesign Fistula Plug Due to Early Expiration
Cook Biotech, Inc. is recalling 102 units of Biodesign Fistula Plug C-FPS-0.7 because the products expire prior to the date printed on the labeling.
Product
Biodesign Fistula Plug C-FPS-0.7 - For implantation to reinforce soft tissue for repair of recto-vaginal or anorectal fistulas. Order Number (GPN): G54614
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3188-2024·2024-10-02
CooperSurgical Recalls Silver-Plated Copper Sims Uterine Sound for Incorrect Marking
CooperSurgical is recalling 468 units of Silver-Plated Copper Sims Uterine Sounds because they were laser-marked with the incorrect part number during manufacturing.
Product
Silver-Plated Copper Sims Uterine Sound, Part Number 64-600
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3253-2024·2024-10-02
Cook Biotech Recalls Biodesign Fistula Plugs Due to Expiration Date Errors
Cook Biotech is recalling 93 Biodesign Fistula Plugs because the products expire prior to the expiration date printed on the labeling.
Product
Biodesign Fistula Plug C-FPS-0.4 - For implantation to reinforce soft tissue for repair of recto-vaginal or anorectal fistulas. Order Number (GPN): G54613
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3220-2024·2024-10-02
Karl Storz Hopkins Telescope 6 endoscope recalled for unapproved reprocessing instructions
Karl Storz is recalling the Hopkins Telescope 6 endoscope because its Instructions for Use contain reprocessing procedures that have not been FDA-reviewed or approved. The recall affects 1,982 units distributed nationwide.
Product
Karl Storz - Endoskope , REF: 27292AMA, Hopkins Telescope 6, Rx only, CE 0123
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3261-2024·2024-10-02
Biodesign Inguinal Hernia Graft Recall Due to Premature Expiration
Cook Biotech is recalling Biodesign Inguinal Hernia Graft units because products expire before their labeled expiration date, potentially affecting surgical outcomes.
Product
Biodesign Inguinal Hernia Graft C-IHM-10X15 - To reinforce soft tissues in the inguinal floor to repair inguinal hernias. Order Number (GPN): G46603
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3196-2024·2024-10-02
Philips Ingenia 3.0T CX MRI Machine Carrier Assembly Screws May Loosen
Philips Ingenia 3.0T CX MRI machines may have loose screws in the RF carrier assembly that could protrude and interfere with the tabletop mechanism, potentially delaying patient scans.
Product
Ingenia 3.0T CX - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal structure of the head, body or extremities, in any orientation. (REF) Numbers: 782105
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3225-2024·2024-10-02
Karl Storz Nephroscope Recall Due to Unapproved Reprocessing Instructions
Karl Storz Endoscope nephroscopes (REF: 27840KA) are being recalled because their instructions for use contain reprocessing methods that have not been reviewed or approved by the FDA for safety and efficacy.
Product
Karl Storz - Endoskope , REF: 27840KA, Nephroscope for MIP L, Rx only, CE 0123
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·24V732000·2024-10-01
2021-2024 Porsche Taycan battery short circuit fire risk
Porsche is recalling 2021-2024 Taycan vehicles due to high-voltage battery short circuits that increase fire risk. Dealers will install diagnostic software and replace batteries as needed, advising owners to charge only to 80% capacity until repairs are completed.
Product
PORSCHE — PORSCHE TAYCAN
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V729000·2024-10-01
Ram 1500 Recalled for Turn Signal Self-Canceling Defect
Chrysler is recalling 2023-2024 Ram 1500 vehicles because the turn signal self-canceling feature may not function properly, increasing crash risk.
Product
RAM — RAM 1500
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24E082000·2024-10-01
Chrysler Recalls Steering Column Modules for Turn Signal Defect
Chrysler is recalling specific MOPAR steering column control modules because the turn signal self-canceling feature may not function properly, increasing crash risk.
Product
EXTERIOR LIGHTING:TURN SIGNAL recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V730000·2024-10-01
Porsche Recalls 2025 Taycan for Delayed Rearview Camera Display
Porsche is recalling 2025 Taycan vehicles because the rearview camera image may not display immediately when shifting into reverse, increasing crash risk.
Product
PORSCHE — PORSCHE TAYCAN
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V733000·2024-10-01
Winnebago motorhomes recalled for defective turn signals
Winnebago Industries recalls multiple motorhome models because turn signals may have insufficient lens area, making them difficult for other drivers to see and increasing crash risk. Dealers will replace the turn signals at no cost.
Product
ITASCA — ITASCA, WINNEBAGO ELLIPSE, SOLEI, TRIBUTE, GRAND TOUR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V734000·2024-10-01
2025 International HX and LT vehicles recalled for fuel pump fracture risk
Navistar is recalling 2025 International HX and LT vehicles with Cummins X15 diesel engines due to fuel pump barrel fracture risk. The fracture can cause fuel leaks and engine stalls, increasing crash risk.
Product
INTERNATIONAL — INTERNATIONAL HX, LT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V736000·2024-10-01
2025 Daimler Trucks Fuel Pump Barrel Fracture Recall
Daimler Trucks North America is recalling certain 2025 commercial trucks with Cummins fuel pumps that may fracture and leak fuel, potentially causing engine stall. No injuries have been reported.
Product
WESTERN STAR — WESTERN STAR, FREIGHTLINER, FCCC 49X, CASCADIA, XCM, XCP
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V731000·2024-10-01
2020-2023 Porsche Taycan Recalled for High-Voltage Battery Short Circuit Risk
Porsche is recalling 2020-2023 Taycan vehicles due to a potential short circuit in the high-voltage battery that increases fire risk. Owners should limit charging to 80% until dealers replace the affected battery modules.
Product
PORSCHE — PORSCHE TAYCAN
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V735000·2024-10-01
Navistar Recalls 2025 International CV Vehicles Due to Inactive Air Bags
Navistar is recalling 2025 International CV vehicles because air bag modules may not have been activated during installation, increasing injury risk in crashes.
Product
INTERNATIONAL — INTERNATIONAL CV
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V728000·2024-09-30
Can-Am Recalls 2017-2019 Spyder RT and F3 Motorcycles for Output Shaft Defect
Bombardier is recalling 2017-2019 Can-Am Spyder RT and F3 motorcycles because the engine output shaft may break, causing a loss of drive power and increasing crash risk.
Product
CAN-AM — CAN-AM SPYDER RT, SPYDER F3
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V727000·2024-09-30
Nova Bus control unit software crash can cut drive power
Nova Bus is recalling certain 2022-2023 LFS buses because a software error may cause the Vehicle Control Unit to crash, disconnecting the high voltage batteries and causing a loss of drive power.
Product
NOVA BUS — NOVA BUS LFS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V726000·2024-09-30
Audi e-tron GT high voltage battery module can short circuit
Audi is recalling certain 2022-2024 e-tron GT and RS e-tron GT vehicles because the high-voltage battery may experience a short circuit within the battery module, increasing fire risk.
Product
AUDI — AUDI RS E-TRON GT, E-TRON GT
Category
Vehicle
Distribution
Distributed nationwide