The Recall Desk

State

New Jersey product recalls

73,817 recalls have nationwide distribution and so reach New Jersey. 9,782 additional recalls listed New Jersey specifically in their distribution scope.

What the numbers show

Total
9,782
Critical
1,246
Severe
2,944
Most recent
2026-11-04

Of the 9,782 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 2,944 (30%) are Severe.

Which agencies issued them

These figures cover only the 9,782 recalls whose distribution notice names New Jersey specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

40551–40575 of 83599

  • HighFDA (Devices)·Z-0688-2019·2019-01-09

    Ortho-Clinical Diagnostics Recalls VITROS HBeAg Reagent Due to Biased Results

    Ortho-Clinical Diagnostics is extending a 2018 recall of VITROS HBeAg Reagent because biotin interference may cause inaccurate test results.

    Product
    VITROS HBeAg Reagent, Cat. No 6801819 Product Usage: For the in vitro qualitative detection of hepatitis B e antigen (HBeAg) in human adult and pediatric (2 to 21 years old) serum from individuals who have symptoms of hepatitis or who may be at risk for hepatitis B virus…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0689-2019·2019-01-09

    Ortho-Clinical Diagnostics Recalls VITROS NT-proBNP Reagent for Biased Results

    Ortho-Clinical Diagnostics is extending a 2018 recall of VITROS NT-proBNP Reagent because it may produce biased results at low biotin concentrations.

    Product
    VITROS NT-proBNP Reagent, Cat No. 6802156 Product Usage: For in vitro diagnostic use only. For the quantitative measurement of N-terminal pro Brain Natriuretic Peptide (NT-proBNP) in human serum and plasma (EDTA or heparin) using the VITROS ECi/ECiQ Immunodiagnostic Systems…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0687-2019·2019-01-09

    Ortho-Clinical Diagnostics Recalls VITROS Anti-HBe Reagent Packs

    Ortho-Clinical Diagnostics is recalling VITROS Anti-HBe Reagent Packs because biased results may occur at lower biotin concentrations than indicated in the instructions.

    Product
    VITROS Anti-HBe Reagent Pack, Cat No. 6801816 Product Usage: For the in vitro qualitative detection of antibodies to hepatitis B e antigen (anti-HBe) in human adult and pediatric (2 to 21 years old) serum from individuals who have symptoms of chronic hepatitis and those who…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0346-2019·2019-01-09

    Lupin Recalls Subpotent Nitrofurantoin Oral Suspension Lots

    Lupin Pharmaceuticals is recalling specific lots of Nitrofurantoin Oral Suspension because the drug was found to contain less active ingredient than required.

    Product
    NITROFURANTOIN — NITROFURANTOIN (NITROFURANTOIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0690-2019·2019-01-09

    Ultradent Recalls Enamelast Fluoride Varnish Due to Off-Flavor Complaints

    Ultradent Products, Inc. is recalling specific lots of Enamelast 5% Sodium Fluoride Varnish because the product may have an unpleasant or off flavor.

    Product
    Enamelast Cool Mint/OT Varnish 5% NaF Mint Label Enamelast Unit Dose 200pk Cool Mint: Enamelast 5% Sodium Fluoride Unit Dose 200pk Kit - Cool Mint REF/UP 4352 Rx CONTENTS: 200 x 0.4 ml Unit Dose Label Enamelast Unit Dose 50pk Cool Mint: Enamelast 5% Sodium…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0691-2019·2019-01-09

    R&D Systems Recalls Human sTfR ELISA Kits Due to Incorrect Control Card

    R&D Systems is recalling 198 Human sTfR ELISA kits because they were packed with the wrong control data card number.

    Product
    Quantikine¿ IVD¿ ELISA, Human sTfR Immunoassay kit. Product Usage: The QuantikineTM IVDTM sTFR Enzyme linked immunosorbent assay is intended for the measurement of sTfR concentration in human serum or plasma as an aid in the diagnosis of iron deficiency anemia, especially…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V004000·2019-01-08

    Daimler Recalls 2014-2017 Sprinter Vans Due to Air Bag Inflator Defect

    Daimler Vans USA is recalling 2014-2017 Freightliner and Mercedes-Benz Sprinter vans because passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 3500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V003000·2019-01-08

    Daimler Recalls 2015-2017 Sprinter Vehicles Due to Air Bag Inflator Defect

    Daimler Vans USA is recalling 2015-2017 Freightliner and Mercedes-Benz Sprinter 2500 and 3500 vehicles because driver air bag inflators may explode during deployment.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 3500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V027000·2019-01-07

    MCI Coaches Recalled for Hydraulic Steering System Locking Risk

    Motor Coach Industries is recalling specific 1997-2015 coaches because a steering defect may cause loss of control at highway speeds.

    Product
    MCI — MCI 102EL3, E4500, J4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V026000·2019-01-07

    Keystone Recalls Dutchmen Travel Trailers Due to Tire Clearance Issue

    Keystone RV is recalling 2017-2019 Dutchmen Voltage and 2019 Endurance travel trailers because tires may contact the rear floor support, affecting handling.

    Product
    DUTCHMEN — DUTCHMEN VOLTAGE, ENDURANCE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V001000·2019-01-07

    Ford Recalls Vehicles for Air Bag Inflator Explosion Risk

    Ford is recalling specific 2010-2014 models because passenger air bag inflators may explode due to humidity, posing a serious injury risk.

    Product
    FORD — FORD, LINCOLN, MERCURY MUSTANG, RANGER, EDGE, MKX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19E004000·2019-01-06

    WSB SC101 Motorcycle Helmets Recalled for Impact Protection Failure

    WSB Inc is recalling SC101 half-helmets manufactured in January 2018 because they may not adequately protect the wearer's head during an impact.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V025000·2019-01-04

    Vantage AMS Edge II Recalled for Fuel Leak Fire Risk

    Vantage Mobility International is recalling 2014-2017 AMS Edge II vehicles because a deteriorating fuel pump gasket may cause fuel leaks, increasing fire risk.

    Product
    VANTAGE — VANTAGE AMS EDGE II
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·19E003000·2019-01-02

    Takata Frontal Passenger Air Bag Inflator Recall for 2010+ Vehicles

    Takata is recalling specific frontal passenger air bag inflators in 2010 or newer vehicles registered in 22 states due to a risk of explosion.

    Product
    AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V022000·2019-01-02

    Pierce Aerial Vehicles Recalled for Unexpected Ladder Rotation Defect

    Pierce Manufacturing is recalling 2004-2018 aerial vehicles because the aerial device may unexpectedly rotate right during extension, increasing injury risk.

    Product
    PIERCE — PIERCE QUANTUM, VELOCITY, IMPEL, ENFORCER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0683-2019·2019-01-02

    Medtronic MiniMed Insulin Pumps Recalled for Missing Audio Alerts

    Medtronic is recalling specific MiniMed insulin pump models because software version 4.10 may fail to play expected audio sounds during alerts, alarms, or sirens.

    Product
    Medtronic MiniMed 630G 6025805-003_C, Rx Only Medtronic MiniMed 670G 6025805-005_B, Rx Only Medtronic MiniMed 640G (International)
    Category
    Medical Device
    Distribution
    52 states
  • HighFDA (Devices)·Z-0674-2019·2019-01-02

    Tosoh Bioscience Recalls ST AIA-PACK Testosterone Diagnostic Test Kits

    Tosoh Bioscience is voluntarily recalling ST AIA-PACK Testosterone kits due to a Class II defect. The recall covers 26,745 units distributed nationwide.

    Product
    ST AIA-PACK Testosterone (TES) is designed for IN VITRO DIAGNOSTIC USE ONLY for the quantitative measurement of testosterone in human serum on specific Tosoh AIA System analyzers. Measurement of testosterone is used to aid in the diagnosis and management of conditions involving…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0663-2019·2019-01-02

    ICU Medical Recalls Iced Thermoset Closed-Loop Injectate Delivery Systems

    ICU Medical is recalling Iced Thermoset Closed-Loop Injectate Delivery Systems due to a defect in the thermoset check valve that may cause leakage.

    Product
    Iced Thermoset Closed-Loop Injectate Delivery System for cold Injectate. 1 unit per Cavity #2-4"x9" Cav/20 pieces per case R1-15645
    Category
    Medical Device
    Distribution
    31 states
  • HighFDA (Devices)·Z-0661-2019·2019-01-02

    ICU Medical Recalls Thermoset Room Temperature Injectate Delivery Systems

    ICU Medical is recalling 27,250 Thermoset Room Temperature Closed Loop Injectate Delivery Systems due to a defect in the thermoset check valve component that may cause leakage.

    Product
    Thermoset Room Temperature Closed Loop Injectate Delivery System. 1 unit per Cavity #3 Cavity Deep/20 pieces per case R1-6090
    Category
    Medical Device
    Distribution
    31 states
  • HighFDA (Devices)·Z-0682-2019·2019-01-02

    Radiometer ABL800 Analyzer Recalled for Potential Patient Data Mismatch

    Radiometer America Inc is recalling 2,131 ABL800 analyzers because software may cause a mismatch between patient demographics and test results.

    Product
    ABL800 analyzer, model numbers 393-800 and 393-801.
    Category
    Medical Device
    Distribution
    Distributed nationwide