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.

40426–40450 of 83599

  • LowFDA (Devices)·Z-0777-2019·2019-02-06

    Riverpoint Medical Recalls 18G Brachy Grids for Incorrect CE Labeling

    Riverpoint Medical is recalling 443 units of 18G Brachy Grids because they are labeled with a CE mark despite not being approved in the European Union.

    Product
    RP RIVERPOINT MEDICAL 18G Brachy Grid B&K(TM) style, REF RPG-18 Product Usage: The Riverpoint Brachytherapy Grid is used during Brachytherapy procedures to assist with the precise insertion of the needle or other probes. The Riverpoint Brachytherapy Grid is placed against…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·013-2019·2019-02-05

    Richwell Group Recalls Frozen Sheat Fish Products for Import Violation

    Richwell Group is recalling approximately 73,360 pounds of frozen Sheat fish products that were imported from Vietnam without the required benefit of import inspection.

    Product
    Richwell Group, Inc. Recalls Siluriformes Products Produced Without Benefit of Import Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V063000·2019-02-05

    Hyundai Recalls 2011-2013 Tucson Models for Engine Oil Pan Leak

    Hyundai is recalling 2011-2013 Tucson vehicles because the engine oil pan may leak, potentially causing engine damage, fire, or stalling.

    Product
    HYUNDAI — HYUNDAI TUCSON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V067000·2019-02-05

    RAM Recalls 2019 Ram 1500 Trucks Due to Brake Pedal Defect

    Chrysler is recalling 2019 Ram 1500 trucks with adjustable pedals because the brake pedal may separate from the assembly, increasing crash risk.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V068000·2019-02-05

    Fiat 124 Spider Recall for Transmission Software Defect

    Chrysler is recalling 2017-2019 Fiat 124 Spider vehicles with automatic transmissions due to a software defect that may cause unexpected downshifting and sudden deceleration.

    Product
    FIAT — FIAT 124 SPIDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19E007000·2019-02-05

    Indian Motorcycle Recalls Scout Models Due to Brake Lever Defect

    Indian Motorcycle is recalling Scout and Scout Bobber models because an accessory brake lever may apply the front brake unintentionally, increasing crash risk.

    Product
    INDIAN — INDIAN SCOUT BOBBER, SCOUT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19059·2019-02-05

    DeWALT Recalls DWD110 and DWD112 Drills Due to Shock Hazard

    DeWALT is recalling DWD110 and DWD112 drills because internal wiring can contact moving parts, posing a shock hazard. No injuries have been reported.

    Product
    DeWALT DWD110 and DWD112 drills
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V071000·2019-02-01

    Ford Recalls 2019 Rangers for Transmission Shift Interlock Defect

    Ford is recalling 2019 Ranger vehicles with 10-speed automatic transmissions because the shift lever can move from Park without the key or brake pedal, risking unexpected movement.

    Product
    FORD — FORD RANGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V070000·2019-01-31

    Mercedes-Benz Recalls 2019 Sprinter VS30 for Steering Shaft Defect

    Daimler Vans is recalling 2019 Mercedes-Benz Sprinter VS30 vehicles because the steering shaft may disconnect, causing a sudden loss of steering control.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER (VS30)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V073000·2019-01-31

    Life Line Recalls 2017-2019 Ambulances Due to Brake Light Wiring Issue

    Life Line Emergency Vehicles is recalling 2017-2019 Type I and Type III ambulances because Whelen accessory brake lights may falsely illuminate, potentially confusing other drivers.

    Product
    LIFELINE — LIFELINE TYPE I, TYPE III
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0737-2019·2019-01-30

    Draeger Medical Recalls VentStar Basic 250 Breathing Circuits Due to Assembly Error

    Draeger Medical is recalling 170 units of VentStar Basic 250 breathing circuits because they were incorrectly pre-assembled, creating a risk of incorrect connection or short circuiting.

    Product
    VentStar Basic 250, Catalog Number MP00350 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only. Breathing Circuits/Anesthesia Sets…
    Category
    Medical Device
    Distribution
    12 states
  • SevereFDA (Devices)·Z-0736-2019·2019-01-30

    Draeger Medical Recalls VentStar Basic 180 Breathing Circuits

    Draeger Medical is recalling 325 units of VentStar Basic 180 breathing circuits due to incorrect pre-assembly that may cause incorrect connections.

    Product
    VentStar Basic 180, Catalog Number MP00349 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only. Breathing Circuits/Anesthesia Sets…
    Category
    Medical Device
    Distribution
    12 states
  • SevereFDA (Devices)·Z-0738-2019·2019-01-30

    Draeger Medical Recalls VentStar Basic Breathing Circuits Due to Assembly Error

    Draeger Medical is recalling 525 units of VentStar Basic (P) 180 breathing circuits because they were incorrectly pre-assembled, posing a risk of incorrect connection or short circuiting.

    Product
    VentStar Basic (P) 180, Catalog Number MP00351 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only. Breathing Circuits/Anesthesia…
    Category
    Medical Device
    Distribution
    12 states
  • SevereFDA (Drugs)·D-0383-2019·2019-01-30

    Bound Tree Medical Recalls Epi Safe Kits Due to Incorrect Instructions

    Bound Tree Medical is recalling Epi Safe Administration and Training Kits because the instructions recommend an unapproved epinephrine dosage for young children.

    Product
    curaplex Epi Safe Administration and Training Kits, #8600-01100, Contains: 2 Epi Safe Administration Kit (8600-01101), 1 Epi Safe Training Kit (8600-01102), Rx Only, Distributed by Sarnova HC, LLC s family of companies: Bound Tree Medical, LLC, Cardio Partners, Inc., Emergency…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0386-2019·2019-01-30

    Bound Tree Medical Recalls Curaplex Epi Kits Due to Incorrect Instructions

    Bound Tree Medical is recalling 339 Curaplex Epi Kits because the instructions recommend an unapproved epinephrine dosage for young children.

    Product
    Curaplex Epi Kit NOT FOR IV USE, #8600-01120, Epi-Safe Kit 8600-01 120 contains:2 Safety-LOK Syringe, TB, 1cc w/ needle, 25 ga x5/8 , 2 Vials of epinephrine, 1mg/1mL, 4 Alcohol prep pads, 2 Adhesive bandages, 1 x 3 1 Epi Generic Injection. Rx Only. Distributed by Sarnova HC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0740-2019·2019-01-30

    Draeger Medical Recalls VentStar Watertrap Breathing Circuits Due to Assembly Error

    Draeger Medical is recalling 25 units of VentStar Watertrap (P) 180 breathing circuits because they were incorrectly pre-assembled, posing a risk of incorrect connection.

    Product
    VentStar Watertrap (P) 180, Catalog Number MP00361 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only. Breathing Circuits/Anesthesia…
    Category
    Medical Device
    Distribution
    12 states
  • SevereFDA (Devices)·Z-0753-2019·2019-01-30

    Teleflex Percuvance Percutaneous Shaft Recall for Potential Tip Breakage

    Teleflex Medical is recalling Percuvance Percutaneous Shafts because the distal tip may deform or break off during use, potentially compromising the tool's security.

    Product
    Percuvance(R) Percutaneous Shaft 29cm, PCVSH3 The Percutaneous Surgical System with 5mm attachments is indicated for the means to penetrate Intended Use: soft tissue to access certain areas of the abdomen. The system is used to grasp, manipulate, cut, cauterize and deliver…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0762-2019·2019-01-30

    Del Monte Fiesta Corn Recalled for Potential Botulism Risk

    Del Monte is recalling Fiesta Corn seasoned with Red & Green Peppers because incorrect thermal processing may allow Clostridium botulinum growth.

    Product
    Del Monte Quality Fresh Cut Harvest Selects Fiesta Corn seasoned with Red & Green Peppers. NET WT 15.25 oz. (432 g); UPC 0 24000 02770; Ingredient: Vegetables (corn, red and green peppers) water, sea salt. Distributed by Del Monte Foods, Walnut Creek, CA 94598
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Devices)·Z-0754-2019·2019-01-30

    Teleflex Percuvance Percutaneous Shaft Recall Due to Tip Breakage Risk

    Teleflex Medical is recalling 1,962 units of Percuvance Percutaneous Shafts because the distal tip may deform or break off during use, potentially requiring surgical intervention.

    Product
    Percuvance(R) Percutaneous Shaft 36cm, PCVSHL3 The Percutaneous Surgical System with 5mm attachments is indicated for the means to penetrate Intended Use: soft tissue to access certain areas of the abdomen. The system is used to grasp, manipulate, cut, cauterize and deliver…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0742-2019·2019-01-30

    Draeger Medical Recalls ID Circuit Watertrap Breathing Circuits Due to Assembly Error

    Draeger Medical is recalling 25 units of ID Circuit Watertrap breathing circuits because they were incorrectly pre-assembled, creating a risk of incorrect connection or short circuit.

    Product
    ID Circuit Watertrap (P) 180, Catalog Number MP01341 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only. Breathing…
    Category
    Medical Device
    Distribution
    12 states
  • SevereFDA (Devices)·Z-0744-2019·2019-01-30

    Draeger ID Circuit Basic 180 Breathing Circuits Recalled for Assembly Defect

    Draeger Medical is recalling 25 units of ID Circuit Basic 180 breathing circuits due to incorrect pre-assembly that may cause connection errors.

    Product
    ID Circuit Basic 180, Catalog Number MP01350 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only. Breathing Circuits/Anesthesia Sets…
    Category
    Medical Device
    Distribution
    12 states