The Recall Desk

State

New Jersey product recalls

73,584 recalls have nationwide distribution and so reach New Jersey. 9,773 additional recalls listed New Jersey specifically in their distribution scope.

What the numbers show

Total
9,773
Critical
1,249
Severe
2,939
Most recent
2026-10-14

Of the 9,773 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 9,773 recalls whose distribution notice names New Jersey specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

476–500 of 83357

  • ModerateFDA (Devices)·Z-3236-2026·2026-09-30

    Philips Ingenia MRI Software Recall for Image Reconstruction Failure

    Philips is recalling 2,038 Ingenia 1.5T MRI systems worldwide due to a software issue that can terminate examinations during image reconstruction if specific scan parameters are manually adjusted.

    Product
    Ingenia 1.5T, Ingenia 1.5T CX and Ingenia 1.5T S; Model Numbers (REF): 1. 781315(1.5T), 2. 781341(1.5T), 3. 781396(1.5T), 4. 782101(1.5T), 5. 782115(1.5T), 6. 782140(1.5T), 7. 781261(1.5T CX), 8. 781262(1.5T CX), 9. 781347(1.5T S);
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3263-2026·2026-09-30

    Baxter PRO+ 36-inch Mattress Recalled for UDI Labeling Error

    Baxter Healthcare is recalling 824 PRO+ 36-inch MRS Surface mattresses due to errors in the Unique Device Identification (UDI) label. The discrepancies may lead to incorrect product identification or use with incompatible bed frames.

    Product
    PRO+ 36" MRS SURFACE, mattress with Advanced Microclimate Technology (AMT) uses a non-powered system of intake and output valves to provide weight-based pressure redistribution whenever a patient moves or is repositioned, Model/Catalog Number: P7924A13
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3261-2026·2026-09-30

    AVID Medical Recalls Halyard IV Start Kits Due to Packaging Seal Issues

    AVID Medical is recalling 192 Halyard IV Start Kits because the included BD ChloraPrep applicators may have open or incomplete packaging seals.

    Product
    Halyard IV START KIT NON-STERILE; 48 kits per case. Containing BD ChloraPrep Clear - 1 mL Applicator. Kit Model Number: KRIV26-01
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3243-2026·2026-09-30

    Philips MRI Software Recall for Image Reconstruction Failure

    Philips is recalling SmartPath MRI software due to a defect that can terminate examinations during image reconstruction if system memory is exceeded.

    Product
    SmartPath to dStream for 1.5T, SmartPath to dStream for 3.0T, SmartPath to dStream for XR and 3.0T, SmartPath to Ingenia Elition X; Model Numbers (REF): 1. 781260 (1.5T), 2. 782112 (1.5T), 3. 782146 (1.5T), 4. 782145 (3.0T), 5. 781270 (XR and 3.0T), 6. 782113 (XR and 3.0T), 7.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3234-2026·2026-09-30

    Philips Achieva XR MRI Systems Recalled for Software Memory Issue

    Philips is recalling 15 Achieva XR MRI systems because a software issue can terminate examinations if scan parameters exceed system memory.

    Product
    Achieva XR; Model Numbers (REF): 1. 781153, 2. 781253;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3239-2026·2026-09-30

    Philips Ingenia MRI Software Recall for Image Reconstruction Failure

    Philips is recalling 596 Ingenia Elition MRI systems due to a software issue that can terminate examinations during image reconstruction if system memory is exceeded.

    Product
    Ingenia Elition S and Ingenia Elition X; Model Numbers (REF): 1. 781357(S), 2. 782106(S), 3. 782137(S), 4. 781358(X), 5. 782107(X), 6. 782119(X), 7. 782136(X), 8. 782158(X);
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-1394-2026·2026-09-30

    So Delicious Dairy Free Salted Caramel Cluster Cashewmilk Recalled for Foreign Material

    WWF Operating Company is recalling So Delicious Dairy Free Salted Caramel Cluster Cashewmilk because it may contain small stones and other hard objects.

    Product
    So Delicious Dairy Free Salted Caramel Cluster Cashewmilk, Non-Dairy Frozen Dessert. 16 oz paper tub with an attached paper lid. Sold as a single unit multi serving tub. UPC 744473 476138. Distributed by For So Delicious Dairy Free Eugene, OR 97402.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3260-2026·2026-09-30

    AVID Medical Recalls Halyard IV Start Kits Due to Packaging Seal Issues

    AVID Medical is recalling Halyard IV Start Kits because the included BD ChloraPrep applicators may have open or incomplete packaging seals.

    Product
    Halyard IV START KIT NON-STERILE; 48 kits per case. Containing BD ChloraPrep Clear - 1 mL Applicator. Kit Model Number: KRIV26-02
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3221-2026·2026-09-30

    Ventec HomeFill Oxygen Cylinder Recall for Missing Medical Gas Labeling

    Ventec Life Systems is recalling 21 HomeFill Oxygen System cylinders because they lack required medical gas labeling.

    Product
    HF2P0ST9 HomeFill Oxygen System HomeFill Cylinder M9 with CGA870 Compatible Post Valve
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0867-2026·2026-09-30

    Macleods Recalls Olanzapine Tablets Due to Impurity Levels

    Macleods Pharmaceuticals is recalling Olanzapine 5 mg tablets because organic and unspecified impurities exceeded specifications.

    Product
    OLANZAPINE — OLANZAPINE (OLANZAPINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V622000·2026-09-29

    Chrysler Recalls 2026 Ram 1500 Vehicles for Side Air Bag Defect

    Chrysler is recalling 2026 Ram 1500 vehicles because side air bag connectors may not be secured properly, potentially preventing deployment in a crash.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V623000·2026-09-29

    RAM Recalls 2026 Ram 1500 Vehicles for Tire Pressure Sensor Defect

    Chrysler is recalling 2026 Ram 1500 vehicles because tire pressure sensors may fail to detect low pressure or illuminate the warning light, increasing crash risk.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V621000·2026-09-29

    Ram Promaster Recall Issued for Electric Power Steering Wiring Defect

    Chrysler is recalling 2022-2026 Ram Promaster and 2024-2026 Ram 3500 Electric vehicles because water may enter the steering wiring harness, potentially disabling power steering assist.

    Product
    RAM — RAM PROMASTER, PROMASTER BEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V619000·2026-09-28

    Volvo Recalls VNL and VNR Trucks for Braking Software Defect

    Volvo Trucks North America is recalling 2025-2027 VNL and 2026-2027 VNR trucks with tanker packages due to inaccurate axle load calculations that may reduce braking performance.

    Product
    VOLVO — VOLVO VNL (4), VNR (4)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26E066000·2026-09-28

    Cummins Recalls L9 Diesel Engines Due to Fuel Hose Separation Risk

    Cummins is recalling L9 diesel engines because remote fuel filter hoses may separate, causing fuel leaks, engine stalls, and increased fire or crash risks.

    Product
    FUEL SYSTEM, DIESEL:DELIVERY:HOSES, LINES/PIPING, AND FITTINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·024-2026·2026-09-25

    Sempio Recalls Ready-to-Eat Chicken Stew Imported Without Reinspection

    Sempio Food Services is recalling ready-to-eat chicken stew products imported from Korea without required reinspection. No illnesses have been reported.

    Product
    Sempio Food Services Inc. Recalls Ready-To-Eat Chicken Stew Products Imported Without the Benefit of Import Reinspection
    Category
    Food
    Distribution
    8 states
  • SevereNHTSA·26V618000·2026-09-25

    ATC Recalls RM900 and RM700 Trailers Due to Coupler Bolt Loosening

    ATC is recalling 2024-2026 RM900 and 2026 RM700 trailers because coupler mounting bolts may loosen, potentially separating the coupler and increasing crash risk.

    Product
    ATC — ATC RM900, RM700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·26797·2026-09-24

    INMO Air3 Smart Glasses Recalled for Overheating Burn Hazard

    INMO International Technology Limited is recalling INMO Air3 Smart Glasses because the left temple can overheat, posing a risk of serious injury or death from burns.

    Product
    INMO AIR3 Smart Glasses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26799·2026-09-24

    ABC Trading Recalls Light-Up Children's Toys Due to Battery Ingestion Risk

    ABC Trading is recalling light-up glasses, headbands, and ties because accessible button cell batteries pose a risk of serious injury or death if swallowed.

    Product
    Light-Up Glasses, Crown Headbands, Sparkle Headbands and Ties
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26792·2026-09-24

    NEWDERY Power Banks Recalled for Fire and Burn Hazards

    NEWDERY is recalling ZHX-PB22 power banks sold on Amazon due to fire and burn hazards. The lithium-ion batteries can explode or ignite, posing a risk of serious injury.

    Product
    NEWDERY power banks
    Category
    Consumer Product
    Distribution
    Distributed nationwide