The Recall Desk

State

New Jersey product recalls

20,096 recalls have nationwide distribution and so reach New Jersey. 0 additional recalls listed New Jersey specifically in their distribution scope.

About recalls in New Jersey

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect New Jersey consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

6476–6500 of 20096

  • HighNHTSA·23V369000·2025-01-05

    Jaguar I-PACE Battery Overheat May Increase Fire Risk

    Jaguar is recalling certain 2019-2024 I-PACE vehicles because the high-voltage battery may overheat, increasing the risk of fire. Owners should park and charge vehicles outside until repairs are complete.

    Product
    JAGUAR — 2021 JAGUAR I-PACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V367000·2025-01-05

    2023 Cadillac Lyriq Battery Connection Defect May Cause Loss of Drive Power

    General Motors is recalling certain 2023 Cadillac Lyriq and 2022 GMC Hummer EV vehicles. Connections in the high-voltage battery pack may be out of position or incorrectly welded, potentially causing loss of drive power and increasing crash risk.

    Product
    CADILLAC — 2023 CADILLAC LYRIQ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V371000·2025-01-05

    IC Bus school buses recalled for ABS warning light failure

    IC Bus school buses (2021–2024) are being recalled because the anti-lock brake system warning light fails to illuminate during malfunctions, preventing drivers from being alerted and increasing crash risk.

    Product
    IC BUS — 2023 IC BUS CESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V292000·2025-01-04

    2023 Subaru Impreza Brake Light Switch and Transmission Interlock Defect

    Subaru is recalling certain 2023 Impreza vehicles due to a faulty brake light switch that may illuminate brake lights without pedal application and allow the transmission to shift out of PARK without pressing the brake pedal, creating rollaway and crash risk.

    Product
    SUBARU — 2023 SUBARU IMPREZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V293000·2025-01-04

    2022 Indian Chief Dark Horse motorcycles recalled for missing belt guard reflectors

    Indian Motorcycle Company is recalling certain 2022 Indian Chief motorcycles that lack belt guard reflectors, which reduces visibility and increases crash risk. All affected vehicles have been remedied.

    Product
    INDIAN — 2022 INDIAN CHIEF DARK HORSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V202000·2025-01-04

    2025 BMW vehicles recalled for loose starter-generator connection defect

    BMW is recalling certain 2025 BMW vehicles because the electrical connection between the starter-generator and battery may come loose, potentially causing engine stall or fire.

    Product
    BMW — 2025 BMW 330I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V106000·2025-01-02

    2024 Hyundai Palisade Engine Valve Springs May Break While Driving

    Hyundai is recalling certain 2024 Palisade vehicles because engine valve springs may break while driving, potentially causing loss of drive power and engine block damage. This increases the risk of crashes and fires.

    Product
    HYUNDAI — 2024 HYUNDAI PALISADE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25081·2025-01-02

    Euqee Wintergreen Essential Oil Recalled for Unsafe Packaging

    Euqee Wintergreen Essential Oils sold on Amazon.com are recalled because their packaging is not child-resistant, violating federal law. Methyl salicylate in the oil could poison young children if swallowed.

    Product
    Euqee Wintergreen Essential Oils
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25082·2025-01-02

    Yaomiao Children's Jewelry Sets Recalled for Dangerous Lead and Cadmium Levels

    Yaomiao children's jewelry sets sold on Amazon contain dangerous levels of lead and cadmium. Consumers should stop using them immediately, keep them away from children, and request a refund from the seller.

    Product
    Yaomiao Children's Jewelry Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25083·2025-01-02

    John Deere ZTrak Zero-Turn Mowers Recalled for Fire and Burn Hazards

    Kawasaki is recalling about 39,000 John Deere ZTrak zero-turn mowers with Kawasaki engines because the voltage regulator can fail, causing the engine to overheat and creating fire and burn hazards. No injuries have been reported to date.

    Product
    John Deere ZTrak™ Zero Turn Mowers with Kawasaki Engines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V108000·2025-01-02

    2023 CFMOTO 450SS Motorcycle Telematics Box Fall May Cause Steering Loss

    CFMOTO is recalling certain 2023 450SS motorcycles where the telematics box may fall onto the steering forks, causing loss of steering control and increasing crash risk. Dealers will replace the T-box holder at no charge.

    Product
    CFMOTO — 2023 CFMOTO 450SS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V026000·2025-01-01

    2022-2023 BMW i4 and iX Vehicles Lack Pedestrian Warning Sounds

    BMW is recalling 2022-2023 i4 eDrive40 and iX xDrive50 electric vehicles because the external pedestrian warning sound system may fail during start-up. Pedestrians could be unaware of approaching vehicles, increasing injury risk.

    Product
    BMW — 2023 BMW I4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0681-2025·2025-01-01

    Glucose Hospital Meter Software Bug Transmits Inaccurate Results

    StatStrip Glucose Hospital Meter software bug may transmit erroneous glucose values to healthcare systems, potentially leading to incorrect patient treatment. 2,365 units affected nationwide and internationally.

    Product
    StatStrip Glucose Hospital Meter System. Model/Catalog Number: 63685. Prescription use blood glucose meter for near-patient testing.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0708-2025·2025-01-01

    Cardiac Monitoring Software Failed to Properly Route ECG Events

    Braemar Manufacturing's Monitoring Service Application (versions 6.5-7.4) failed to properly route and review ECG events from July 2022-July 2024 due to a disabled analysis step. This affected about 130,000 units with 41,282 customers nationwide.

    Product
    Monitoring Service Application (MSA). Software to process, analyze, display, and report cardiac events in ECG data received from compatible devices.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0683-2025·2025-01-01

    Blood glucose ketone meter software bug causes erroneous result transmission

    Nova Biomedical's StatStrip glucose ketone hospital meter (Model 63910) has a software bug that may transmit erroneous results to healthcare systems. The issue affects 1,615 units distributed across the US and internationally.

    Product
    StatStrip Glucose Ketone (mmol/L) Hospital Meter System. Model/Catalog Number: 63910. Prescription use blood glucose ketone meter for near-patient testing
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0682-2025·2025-01-01

    Blood Glucose Ketone Meter Firmware Bug Causes Inaccurate Test Results

    Software bug in StatStrip Glucose Ketone Hospital Meter System can cause incorrect blood glucose and ketone test results to be transmitted to healthcare data systems. 347 units affected.

    Product
    StatStrip Glucose Ketone Hospital Meter System. Model/Catalog Number: 63683. Prescription use blood glucose ketone meter for near-patient testing
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0759-2025·2025-01-01

    Medline ST IUD Removal Hook Recalled Due to Weak Seals and Sterility Risk

    Medline Industries is recalling 21,440 units of the ST IUD Removal Hook due to weak seals that may compromise sterility. The defect is undetectable to users and could increase infection risk.

    Product
    ST IUD REMOVAL HOOK 10" (504090), Medline Item No. I68785
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0723-2025·2025-01-01

    Medline surgical patties and strips recalled for endotoxin contamination

    Medline surgical patties and strips used in certain procedure convenience kits were found to contain higher-than-expected endotoxin levels that may exceed safety specifications. The affected kits were distributed nationwide and in Canada.

    Product
    Medline brand, medical procedure convenience kits, labeled as: 1) CRANIOTOMY, SKU CDS982719X; 2) MVFF/FIBU #54-RF, SKU DYNJ21927Q; 3) MVFF/FIBU #54-RF, SKU DYNJ21927S; 3) NEURO PEDIATRIC, SKU DYNJ61607A; 4) CRANIOTOMY PACK, SKU DYNJ66419C; 5) LYMPHATIC BYPASS PACK, SKU DYNJ69907;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0718-2025·2025-01-01

    Surgical patties and strips recalled due to endotoxin contamination

    Medline Industries is recalling FESS-MB PACK-LF Convenience kits containing surgical patties and strips due to higher-than-expected endotoxin levels in raw materials, resulting in out-of-specification finished products.

    Product
    FESS-MB PACK-LF Convenience kit, SKU DYNJ0888159I. Convenience kits used for various procedures..
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0740-2025·2025-01-01

    Siemens Blood Analysis Device Recalled Over Patient Name Mix-up Software Defect

    Siemens is recalling the epoc NXS blood analysis system due to a software flaw that can assign incorrect patient names to test results, risking misdiagnosis or mistreatment if the operator doesn't verify the patient name.

    Product
    epoc NXS Host; Siemens Material Number (SMN): 11413583(CN, KR) ; Software Version Number: 4.14.9. Intended for use by trained medical professionals as an in vitro diagnostic device for the quantitative testing of samples of heparinized or un-anticoagulated arterial, venous or
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0753-2025·2025-01-01

    Merlin PCS 3650 Pacemaker Programmer Software Anomaly May Cause Loss of Pacing

    A software anomaly in Abbott's Merlin PCS 3650 programmer may prevent proper finalization of leadless pacemakers, causing loss of pacing function. The issue occurs when specific actions combine with brief telemetry loss.

    Product
    The Merlin PCS 3650 programmer Model 3330 The Merlin PCS programmer model 3650 is a portable, dedicated programming system which operates using the Merlin PCS Model 3330 software and is designed to interrogate, program, display data from, and test Abbott Medical implantable
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0748-2025·2025-01-01

    BD FACSLyric Flow Cytometer Power Supply Module Failure Risk

    BD is recalling power supply modules on FACSLyric flow cytometers that may fail to power on or stay on. Failure could cause lab staff to inhale fumes and patients to need repeat blood draws.

    Product
    FACSLyric 3L10C Instrument US-IVD, Catalog Number 662878, UDI 00382906628787 The K170974 clearance document describes the device as follows: The BD FACSLyric" flow cytometer (3-1, 4-2, 4-2-2, and 4-3-3 optical configurations) systems consist of a flow cytometer, sheath ta
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0755-2025·2025-01-01

    Medline Surgical Scissors Recalled for Sterility Seal Defect

    Medline O.R. scissors may have weak seals that compromise sterility, increasing risk of contamination and infection. Approximately 21,440 units from lot 2023052490 have been recalled nationwide.

    Product
    O.R. SCISSORS, S/B, 5.5 STERILE, Medline Item No. DYND04000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0735-2025·2025-01-01

    Blood analyzer system recalled for patient name assignment software error

    Siemens recalled its epoc NXS Host blood analyzer due to a software malfunction that can assign incorrect patient names to test results, potentially leading to misdiagnosis or mistreatment.

    Product
    epoc NXS Host; Siemens Material Number (SMN): 11413497 (EU); Software Version Number: 4.14.9. Intended for use by trained medical professionals as an in vitro diagnostic device for the quantitative testing of samples of heparinized or un-anticoagulated arterial, venous or capi
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0726-2025·2025-01-01

    Surgical procedure kits recalled for elevated endotoxin levels

    Medline surgical kits containing sterile surgical patties and strips have been recalled due to higher-than-expected endotoxin levels in raw materials. The affected supplies may pose a risk during sterile surgical procedures.

    Product
    Medline brand, medical procedure convenience kits, labeled as: 1) LAMINECTOMY CDS-LF, SKU CDS780045N; 2) NEURO CRANIOTOMY CDS #36-RF, SKU CDS780119U; 3) NEURO CRANIOTOMY CDS #36-RF, SKU CDS780119V; 4) CRANIOTOMY CDS, SKU CDS981753K; 5) LAMINECTOMY CDS-LF, SKU CDS981923X; 6)
    Category
    Medical Device
    Distribution
    Distributed nationwide