The Recall Desk

State

New Jersey product recalls

73,737 recalls have nationwide distribution and so reach New Jersey. 9,780 additional recalls listed New Jersey specifically in their distribution scope.

What the numbers show

Total
9,780
Critical
1,246
Severe
2,942
Most recent
2026-10-28

Of the 9,780 recalls naming New Jersey we have scored against our rubric, 1,246 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,942 (30%) are Severe.

Which agencies issued them

These figures cover only the 9,780 recalls whose distribution notice names New Jersey specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

31251–31275 of 83517

  • HighFDA (Devices)·Z-2987-2020·2020-09-30

    LivaNova Recalls Perceval Single Use Accessory Kits Due to Collapse Failure

    LivaNova is recalling specific lots of Perceval Single Use Accessory Kits because the Dual Collapser component may fail to reduce the heart valve diameter during implantation.

    Product
    Perceval Single Use Accessory Kit, Size M, REF: ICV1350, Sterile EO, Rx Only, CE, UDI: 8022057015259 - Product Usage: he Dual Collapser is a component of the Perceval single use accessory kits used to reduce the Perceval Sutureless heart valve diameter before valve implant…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2995-2020·2020-09-30

    GE Healthcare Recalls NM 830 Medical Detectors Due to Loose Screws

    GE Healthcare is recalling 25 NM 830 detectors because rotor bearing screws were found loose. The devices are distributed in the US and internationally.

    Product
    NM 830 Model # H3910AC
    Category
    Medical Device
    Distribution
    27 states
  • HighFDA (Devices)·Z-2999-2020·2020-09-30

    ArthroCare Speed Stitch Needle Cassettes Recalled for Potential Breakage

    ArthroCare is recalling Speed Stitch Needle Cassettes because a supplier error may have resulted in needles made of titanium instead of stainless steel, posing a risk of breakage during use.

    Product
    Speed Stitch Needle Cassette
    Category
    Medical Device
    Distribution
    42 states
  • ModerateFDA (Devices)·Z-2982-2020·2020-09-30

    Bio-Rad Recalls BioPlex 2200 Syphilis Assay Due to Increased Reactivity

    Bio-Rad is recalling BioPlex 2200 Syphilis Total & RPR kits because of increased RPR reactivity levels in the kit material.

    Product
    BioPlex 2200 Syphilis Total & RPR Linked Immunoabsorption Assay, Treponema pallidum:UDI:03610520653012 - Product Usage: intended for the qualitative detection of total (IgG/IgM) antibodies to Treponema pallidum and the qualitative detection and/or titer determination of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2997-2020·2020-09-30

    GE Healthcare Recalls Discovery NM670 Pro Due to Loose Screws

    GE Healthcare is recalling nine Discovery NM670 Pro units because rotor bearing screws were found loose on the detector.

    Product
    Discovery NM670 Pro Model # H3100XB
    Category
    Medical Device
    Distribution
    27 states
  • ModerateFDA (Devices)·Z-3011-2020·2020-09-30

    Irvine Biomedical Recalls Steerable Diagnostic Catheters Due to Labeling Error

    Irvine Biomedical is recalling 15 units of Inquiry Steerable Diagnostic Catheters because packages were mislabeled with the wrong model and batch numbers.

    Product
    Inquiry Steerable Diagnostic Catheter, REF: IBI-81104 - Product Usage: INDICATIONS FOR USE The Inquiry fixed curve and steerable electrophysiology catheters are used for electrogram recording and cardiac stimulation during diagnostic electrophysiology studies. The catheters are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2983-2020·2020-09-30

    Beckman Coulter Recalls DxA 5000 Automated Sample Handling Systems

    Beckman Coulter is recalling 32 DxA 5000 automated sample handling systems because the instructions for use may be confusing regarding the re-use of sample IDs, leading to undetected barcode re-use.

    Product
    DxA 5000; Catalog Number:B50516; UDI:15099590707118 - Product Usage: The DxA 5000 is a high-speed, modular, automated sample handling system that performs pre-analytical and post-analytical sample processing and storage. The automation system also sorts, routes, and presents…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3006-2020·2020-09-30

    Beckman Coulter Access Unconjugated Estriol Assay Systems Recalled for Interference

    Beckman Coulter is recalling Access Unconjugated Estriol assay systems because alkaline phosphatase interference may cause falsely elevated results.

    Product
    BECKMAN COULTER ACCESS Immunoassay Systems - Access Unconjugated Estriol, REF 33570.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-3001-2020·2020-09-30

    OraSure CVS Advanced Wart Remover Kit Recalled for Improper Sealing

    OraSure Technologies is recalling CVS Advanced Wart Remover Kits because unit boxes were not properly sealed. The recall covers 23,400 units distributed in the US, Canada, and Brazil.

    Product
    CVS Advanced Wart Remover Kit, Catalog Number: 1001-0407 - Product Usage: indicated for over-the-counter a cryosurgical system for the treatment of common warts and plantar warts.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-3002-2020·2020-09-30

    OraSure Personelle OTC Skin Tag Remover Recalled for Improperly Sealed Boxes

    OraSure Technologies is recalling 3,000 units of Personelle OTC Skin Tag Remover because unit boxes were not properly sealed.

    Product
    Personelle OTC Skin Tag Remover, Canada Catalog Number: 1001-0314 - Product Usage: indicated for over-the-counter a cryosurgical system for the treatment of skin tags.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-3003-2020·2020-09-30

    OraSure Pointts Skin Tag Removal System Recalled for Unsealed Boxes

    OraSure Technologies is recalling Pointts skin tag removal systems because unit boxes were not properly sealed. The recall affects 23,220 units distributed in the US, Canada, and Brazil.

    Product
    Pointts sistema de ellmlnact!;o de verrugas OTC - Brazil Catalog Number: 1001-0280 - Product Usage: indicated for over-the-counter a cryosurgical system for the treatment of skin tags.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-3004-2020·2020-09-30

    DNA Genotek PrepIT Q2A Kit Recalled for Expired Reagents

    DNA Genotek Inc. is recalling 74 units of the PrepIT Q2A Kit because reagents were shipped after their expiration dates.

    Product
    PrepIT Q2A Kit, Model PT-Q2A-96 containing component reagent AG (PT-QAG-96) 1.4mL and ST (PT-QST-96) 2.9mL - Product Usage: used for the removal of SDS and other inhibitors from samples collected using DNA Genotek oral sample collection kits.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V595000·2020-09-29

    Mercedes-Benz and Freightliner Sprinter Fuel Line Clamp Recall

    Daimler Vans USA is recalling 2019-2020 Sprinter vans because fuel line clamps may loosen, causing a fuel leak that increases fire risk.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 2500, SPRINTER 3500, SPRINTER 4500, SPRINTER 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V594000·2020-09-29

    2021 Newmar Motorhomes Recalled for Leveling Jack Fastening Defect

    Newmar is recalling certain 2021 motorhome models because the front leveling jacks may not be properly fastened to the chassis. If the jacks fail, the motorhome could unexpectedly drop, creating an injury risk.

    Product
    NEWMAR — NEWMAR ESSEX, DUTCH STAR, MOUNTAIN AIRE, LONDON AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E072000·2020-09-29

    Spartan Fire Recalls Gladiator and MetroStar Vehicles Due to Gauge Defect

    Spartan Fire is recalling 2018-2019 Gladiator and MetroStar vehicles because replacement gauges may prevent the Advanced Protection System from engaging, increasing injury risk in crashes.

    Product
    SPARTAN — SPARTAN, SPARTAN FIRE METROSTAR, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V593000·2020-09-28

    Kenworth T680 Trucks Recalled for Brake System Valve Defect

    PACCAR is recalling 2016-2021 Kenworth T680 trucks because a brake valve defect may increase stopping distance and crash risk.

    Product
    KENWORTH — KENWORTH T680
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V592000·2020-09-28

    Shyft Recalls 2015-2019 Utilimaster Ram ProMaster Fleet Vehicles

    Shyft Group is recalling 2015-2019 Utilimaster Ram ProMaster fleet vehicles because the transmission shifter cable may disconnect, causing unintended vehicle movement.

    Product
    UTILIMASTER — UTILIMASTER RAM PROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V591000·2020-09-25

    2020-2021 Dynamax Isata Motorhomes Recalled for Engine Software Fire Risk

    Forest River is recalling 2020-2021 Dynamax Isata motorhomes due to engine software that fails to provide adequate warmup protection. The defect can cause bearing damage and engine block failure, risking oil leaks and fires.

    Product
    DYNAMAX — DYNAMAX ISATA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V589000·2020-09-25

    2021 Forest River Wildwood RV Cooktop May Pose Fire Risk

    Forest River is recalling 2021 Wildwood and Salem trailers. The cooktop flame may invert due to furnace air leakage, increasing fire risk.

    Product
    FOREST RIVER — FOREST RIVER SALEM, WILDWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide