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.

43201–43225 of 83599

  • LowFDA (Devices)·Z-2384-2018·2018-07-18

    Arrow International Recalls VPS TipTracker Stylet Accessory Due to Labeling Issues

    Arrow International Inc. is recalling 2,070 units of the VPS TipTracker Stylet Accessory because the product pouch label may not easily identify the lot number, expiration date, and associated symbols.

    Product
    VPS TipTracker Stylet Accessory, REF RHY-177-TTSAP Product Usage: To provide real time tip location information of a central venous catheter by utilization of ECG to observe P-wave changes as the tip approaches the right atrium of the heart via the Superior Vena Cava (SVC).…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0978-2018·2018-07-18

    Mylan Recalls Subpotent Triamterene and Hydrochlorothiazide Tablets Nationwide

    Mylan Pharmaceuticals is voluntarily recalling 28,436 bottles of Triamterene and Hydrochlorothiazide Tablets because the medication was found to be subpotent.

    Product
    Triamterene and Hydrochlorothiazide Tablets, USP 37.5 mg/25 mg, 100-count bottle, Rx only, Mylan Pharmaceuticals, Inc. Morgantown, WV 26505, NDC 0378-1352-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0913-2018·2018-07-18

    Wockhardt Recalls Enalapril Maleate Tablets Due to Impurity Failures

    Wockhardt Limited is recalling specific batches of Enalapril Maleate Tablets USP because they failed impurity and degradation specifications.

    Product
    Enalapril Maleate Tablets USP; 2.5 mg NDC code 64679-923-03. 1000 Tablets HDPE container pack with Non CRC cap and 2 desiccants further packed in E-flute cartons.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·063-2018·2018-07-17

    Smithfield Recalls Pepperoni Five Cheese Calzones Due to Plastic Contamination

    Smithfield Packaged Meats is recalling approximately 24,048 pounds of pepperoni five cheese calzones that may contain hard, sharp, clear plastic pieces.

    Product
    Smithfield Packaged Meats Corp. — Smithfield Packaged Meats Corp. Recalls Pepperoni Five Cheese Calzone Products Due to Possible Extraneous Material Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E055000·2018-07-17

    Martinrea Brake Hose Recall for Corrosion-Related Fluid Leak Risk

    Martinrea is recalling brake hose assemblies for Chrysler and Ford vehicles that may lack anti-corrosion plating, posing a risk of brake fluid leaks and reduced braking effectiveness.

    Product
    SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:HOSES, LINES/PIPING, AND FITTINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V473000·2018-07-17

    BMW Recalls 2018 M5 Vehicles Due to Fuel Level Sensor Defect

    BMW is recalling 2018 M5 vehicles because a fuel level sensor may stick to a fuel line, causing inaccurate fuel gauge readings that could lead to stalling and increased crash risk.

    Product
    BMW — BMW M5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E054000·2018-07-16

    TRW Brake Caliper Piston Coating Defect Recall for Multiple Vehicle Brands

    TRW is recalling brake caliper pistons with insufficient coating for vehicles from Volkswagen, Fiat Chrysler, BMW, and Mercedes-Benz to prevent reduced braking performance.

    Product
    SERVICE BRAKES, HYDRAULIC recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V470000·2018-07-16

    Ford Recalls 2018 F53 Chassis Due to Wheel Stud Defect

    Ford is recalling 2018 F53 stripped chassis vehicles because improperly heat-treated front wheel studs may break, increasing crash risk.

    Product
    FORD — FORD F53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V467000·2018-07-13

    Volkswagen Recalls 2018 Tiguan Vehicles Due to Sunroof Fire Risk

    Volkswagen is recalling 2018 Tiguan vehicles because the panoramic sunroof LED module may short circuit, increasing the risk of a fire.

    Product
    VOLKSWAGEN — VOLKSWAGEN TIGUAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·18V468000·2018-07-13

    Forest River Recalls 2019 Palomino Campers Due to Incorrect Weight Label

    Forest River is recalling 2019 Palomino hardside truck campers because the Federal Placard lists an incorrect dry weight, which may result in the vehicle being overloaded.

    Product
    FOREST RIVER — FOREST RIVER PALOMINO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E053000·2018-07-12

    Chrysler and Dodge Vehicles Recalled for Cruise Control Defect

    Chrysler is recalling specific 2014-2018 Chrysler 300, Dodge Charger, and Challenger vehicles because a defect may prevent the cruise control system from disengaging.

    Product
    CHRYSLER — CHRYSLER, DODGE 300, CHARGER, CHALLENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V466000·2018-07-12

    Multiquip Recalls 2018 Trailers Due to Center-Mounted Jack Collapse Risk

    Multiquip is recalling 2018 TRLR45H and TRLR70USH trailers because the center-mounted jack may collapse under excessive load, increasing the risk of injury.

    Product
    MULTIQUIP — MULTIQUIP TRLR45H, TRLR70USH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2347-2018·2018-07-11

    FHC Depth Stop Adapter Recalled for Potential Lead Damage

    FHC, Inc. is recalling the microTargeting Drive System because the Depth Stop Adapter may damage implanted leads if over-tightened, potentially requiring replacement.

    Product
    microTargeting" Drive System, Product Number 66-ZD-MD
    Category
    Medical Device
    Distribution
    46 states
  • SevereFDA (Devices)·Z-2346-2018·2018-07-11

    FHC Depth Stop Adapter Recalled for Lead and Stylet Damage

    FHC, Inc. is recalling the microTargeting Drive System because the Depth Stop Adapter can damage implanted leads and stylets when over-tightened, requiring device replacement.

    Product
    microTargeting" Drive System, Product Number MT-DS-01
    Category
    Medical Device
    Distribution
    46 states
  • SevereFDA (Devices)·Z-2349-2018·2018-07-11

    FHC Depth Stop Adapter Recalled for Potential Lead Damage

    FHC, Inc. is recalling the microTargeting STar Drive System (Manual) because the Depth Stop Adapter may damage the lead and stylet if the screw is over-tightened.

    Product
    microTargeting" STar" Drive System (Manual), Product Number ST-DS-MA
    Category
    Medical Device
    Distribution
    46 states
  • SevereFDA (Devices)·Z-2348-2018·2018-07-11

    FHC Depth Stop Adapter Recalled for Lead and Stylet Damage

    FHC, Inc. is recalling the microTargeting Drive System because the Depth Stop Adapter can damage leads and stylets, potentially causing short circuits.

    Product
    microTargeting" Drive System, Product Number 66-ZD-MD-01
    Category
    Medical Device
    Distribution
    46 states
  • SevereFDA (Devices)·Z-2352-2018·2018-07-11

    FHC Depth Stop Adapter Recalled for Potential Lead Damage

    FHC, Inc. is recalling the Depth Stop Adapter because over-tightening the screw can damage implanted leads, causing short circuits and requiring replacement.

    Product
    microTargeting" STar" Drive System (Motorized), Product Number 70-ZD-ME
    Category
    Medical Device
    Distribution
    46 states
  • SevereFDA (Devices)·Z-2350-2018·2018-07-11

    FHC Depth Stop Adapter Recall Due to Lead and Stylet Damage

    FHC, Inc. is recalling the Depth Stop Adapter because over-tightening the screw can damage implanted leads and stylets, requiring replacement.

    Product
    microTargeting" STar" Drive System (Motorized), Product Number ST-DS-ME
    Category
    Medical Device
    Distribution
    46 states
  • SevereFDA (Devices)·Z-2359-2018·2018-07-11

    FHC Depth Stop Adapter Recalled for Lead Damage Risk

    FHC, Inc. is recalling Depth Stop Adapters because over-tightening the screw can damage implanted leads, requiring removal and replacement.

    Product
    microtargeting" Depth Stop Adapter, Product Model Number, Product Number 66-AC-DS(1.8),
    Category
    Medical Device
    Distribution
    46 states
  • SevereFDA (Devices)·Z-2356-2018·2018-07-11

    FHC Depth Stop Adapter Recalled for Potential Lead and Stylet Damage

    FHC, Inc. is recalling the microTargeting Drive System Depth Stop Adapter because over-tightening the screw can damage implanted leads, requiring replacement.

    Product
    microTargeting" Drive System Distributed by Medtronic, Product Number 9033G0601
    Category
    Medical Device
    Distribution
    46 states
  • SevereFDA (Drugs)·D-0891-2018·2018-07-11

    Ingenus Recalls Irinotecan Hydrochloride Injection Due to Potency Issues

    Ingenus Pharmaceuticals is recalling Irinotecan Hydrochloride Injection because of high out-of-specification assay values for potency.

    Product
    IRINOTECAN HYDROCHLORIDE — IRINOTECAN HYDROCHLORIDE (IRINOTECAN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide