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.

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.

30426–30450 of 83517

  • HighNHTSA·20V754000·2020-12-07

    2021 East to West Recreational Trailers: Stowed Grill Fire Hazard

    Forest River is recalling 2021 East to West recreational trailers (approximately 115 units). The grill can be stowed with the propane hose attached and burners on, which can increase fire risk.

    Product
    EAST TO WEST — EAST TO WEST DELLA TERRA, SILVER LAKE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V753000·2020-12-04

    Mercedes-Benz A 220 Recalled for Missing Tire Pressure Labels

    Mercedes-Benz is recalling 2019 A 220 vehicles because missing tire pressure labels may lead to incorrect inflation and increased crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ A 220
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V752000·2020-12-04

    E-One Recalls Emergency Vehicles Due to Display Lockup Risk

    E-One is recalling specific 2019-2021 emergency vehicles because LCD displays may lock up, potentially delaying emergency efforts.

    Product
    E-ONE — E-ONE COMMERCIAL, QUEST II, TYPHOON N, CYCLONE II
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V751000·2020-12-03

    Land Rover Recalls 2020 Models for Speedometer Display Software Error

    Land Rover is recalling 2020 Discovery Sport and Range Rover Evoque vehicles because a software error may cause the speedometer to randomly switch units, potentially distracting drivers.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER EVOQUE, DISCOVERY SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21711·2020-12-03

    Honda Recalls Pioneer 700 and 1000 Vehicles Due to Steering Control Issues

    American Honda is recalling approximately 118,600 Pioneer 700 and 1000 vehicles because the electric power steering system may lose control, posing crash and injury hazards.

    Product
    Honda Pioneer 700 & 1000 Recreational Off-Highway Vehicles (ROVs) with Electric Power Steering (EPS)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0133-2021·2020-12-02

    Whole Foods Chicken Rustico Romano Chef Plate Recalled for Undeclared Egg

    Whole Foods Market is recalling Chicken Rustico Romano Chef Plates due to potential undeclared egg. The product was distributed in five states and Washington, D.C.

    Product
    Chicken Rustico Romano Chef Plate with Mac & Cheese and Broccoli, packaged in clear plastic container with printed label product code begins with 241442
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-0132-2021·2020-12-02

    Whole Foods Recalls Fried Chicken Meals for Potential Undeclared Egg

    Whole Foods Market is recalling Fried Chicken Meals with Mac & Cheese in five states and D.C. due to a potential undeclared egg allergen.

    Product
    Fried Chicken Meal with Mac & Cheese, packaged in clear plastic container with printed label product code begins with 247257; Fried Chicken Meal with Mac & Cheese, packaged on hot bar product code begins with 237444
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-0130-2021·2020-12-02

    Whole Foods Market Recalls Macaroni and Cheese for Undeclared Egg

    Whole Foods Market is recalling specific macaroni and cheese products due to a potential undeclared egg allergen. Consumers in five states and D.C. should check their products.

    Product
    Macaroni & Cheese, chef s case; Macaroni & Cheese, packaged in clear plastic container; Macaroni & Cheese, online and catering product code begins with 286501, 263608, 114449, or 109866
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-0135-2021·2020-12-02

    Whole Foods Recalls BBQ Turkey Meatballs for Undeclared Egg

    Whole Foods Market is recalling BBQ Turkey Meatballs Chef Plates due to a potential undeclared egg allergen. The product was distributed in Maryland, New Jersey, Pennsylvania, Virginia, and Washington, D.C.

    Product
    BBQ Turkey Meatballs Chef Plate with Mac & Cheese and Green Beans, packaged in clear plastic container with printed label product code begins with 241464
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-0131-2021·2020-12-02

    Whole Foods Recalls Rotisserie Chicken Meals for Undeclared Egg

    Whole Foods Market is recalling Rotisserie Chicken Meals with Mac & Cheese and Broccoli due to a potential undeclared egg allergen. The recall affects specific product codes sold in the Mid-Atlantic region.

    Product
    Rotisserie Chicken Meals with Mac & Cheese and Broccoli, packaged in clear plastic container with printed label product code begins with 261596 261580, 261590, 261601, 261608, or 261616
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-0134-2021·2020-12-02

    Whole Foods Chicken Breast Chef Plate Recalled for Undeclared Egg

    Whole Foods Market is recalling Chicken Breast Chef Plate with Mac & Cheese and Broccoli due to potential undeclared egg.

    Product
    Chicken Breast Chef Plate with Mac & Cheese and Broccoli, packaged in clear plastic container with printed label product code begins with 299430
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Devices)·Z-0497-2021·2020-12-02

    Flexicare ProVu Video Stylet Recalled for Potential Airway Occlusion

    Flexicare Medical Ltd. is recalling ProVu Single Use Video Stylets with ET Tubes because over-inflated cuffs may block the airway, making it difficult to ventilate patients.

    Product
    ProVu Single Use Video Stylet with ET Tube, Part/Size: 038-990-080U/ 8.0, 038-990-075U/ 7.5, 038-990-070U/ 7.0, 038-990-065U/ 6.5 *Note: product list updated per 12/23/2020 letter to customers
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0103-2021·2020-12-02

    Paroex Oral Rinse Recalled for Burkholderia lata Contamination

    Sunstar Americas is recalling Paroex Oral Rinse due to microbial contamination with Burkholderia lata. The recall covers specific lots distributed nationwide.

    Product
    Paroex (chlorhexidine gluconate) Oral Rinse, USP 0.12%, Alcohol Free, Rx only, packaged in: a) 1 pint (473 mL) NDC 52376-021-02; b) 4 fl oz (118 mL) NDC 52376-021-04, Sunstar Americas, Inc.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0136-2021·2020-12-02

    Whole Foods Recalls Roasted Turkey Chef Plate for Undeclared Egg

    Whole Foods Market is recalling Roasted Turkey Chef Plates with Mac & Cheese and Broccoli due to a potential undeclared egg allergen.

    Product
    Roasted Turkey Chef Plate with Mac & Cheese and Broccoli, packaged in clear plastic container with printed label product code begins with 242019
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-0137-2021·2020-12-02

    GT's Living Foods Recalls Synergy Raw Kombucha Multi-Green

    GT's Living Foods is recalling Synergy raw kombucha Multi-Green due to high levels of microcystins found by FDA sampling.

    Product
    Synergy raw kombucha - Multi-Green; 16 fl. oz. (473 mL) UPC 7 22430 14016 2 GT's Living Foods LLC Beverly Hills, CA
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Devices)·Z-0484-2021·2020-12-02

    Hill-Rom Recalls Life2000 Ventilation Systems Due to Fire Risk

    Hill-Rom is recalling 67 Life2000 Ventilation Systems because they pose a risk of fire under certain conditions. The devices are used in home and institutional settings.

    Product
    Life2000 Ventilation System, including Life2000 Ventilator and Life2000 Compressor, Model MS-01-0118 - Product Usage: use in home and institutional settings and is not intended for ambulance or air transport.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V750000·2020-12-02

    Kia Recalls 294,756 Vehicles for Engine Compartment Fire Risk

    Kia is recalling 294,756 vehicles from 2011-2015 due to a risk of engine compartment fire while driving. Dealers will inspect for leaks and update software.

    Product
    KIA — KIA FORTE KOUP, SOUL, FORTE, SORENTO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0491-2021·2020-12-02

    FDA Recalls Geistlich Bio-Oss Pen Due to Granule Expulsion Risk

    Geistlich Pharma North America is recalling Geistlich Bio-Oss Pen units because granules may be expelled all at once, posing a risk of tissue injury.

    Product
    Geistlich Bio-Oss Pen 0.25-1mm 0.5g - Product Usage: natural bone mineral for filling of bone defects in maxillofacial surgery, implantology, and periodontology. Product Number: 20116
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V749000·2020-12-02

    Audi 2021 A6, Q7, RS6, and RS7 Crash Sensor Electrical Defect

    Volkswagen Group of America (Audi) is recalling 2021 Audi A6, Q7, RS6, and RS7 vehicles. An electrical connector can detach from door crash sensors, potentially delaying restraint system activation during side-impact crashes.

    Product
    AUDI — AUDI RS 6 AVANT, RS 7, A6, Q7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0483-2021·2020-12-02

    Bayer Recalls MEDRAD Stellant FLEX Syringe Kits Due to Cracks

    Bayer Medical Care is recalling specific lots of MEDRAD Stellant FLEX 150 mL syringe kits because they may have holes or cracks that allow fluid to leak.

    Product
    Brand Name: MEDRAD Stellant FLEX Syringe Kits Common Name: Angiographic Syringe Catalog/REF Number: FLEXD-150-SCS Description: 2 - 150 mL FLEX syringes, 1 large saline spike, 1 small contrast spike, patient t-connector tubing & prime tube. Catalog/REF Number…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0482-2021·2020-12-02

    ViewRay MRIdian Linac System Recalled for Potential Burn Injury Risk

    Viewray, Inc. is recalling 35 ViewRay MRIdian Linac Systems because receive coil components may reach elevated temperatures, posing a risk of burn injury to patients or users.

    Product
    ViewRay MRIdian Linac System: Model No. 20000, CE, Rated Supply Voltage - 380/480 VAC, 3 - Frequency Range (Hertz) - 50/60 Hz, Rated Input in Amperes - 210 A, UDI. The MRIdian system and the MRIdian Linac system, with magnetic resonance imaging capabilities, is intended to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0492-2021·2020-12-02

    Geistlich Bio-Oss Pen Recalled Due to Granule Expulsion Risk

    Geistlich Pharma North America is recalling Geistlich Bio-Oss Pen 1-2mm 0.5g units because granules may be expelled all at once, posing a risk of tissue injury.

    Product
    Geistlich Bio-Oss Pen 1-2mm 0.5g - Product Usage: natural bone mineral for filling of bone defects in maxillofacial surgery, implantology, and periodontology. Product Number: 20126
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21039·2020-12-02

    ADCO Recalls Sure Scents Candles Due to Fire and Burn Hazards

    ADCO is recalling Sure Scents 2-1 Peaceful Stream/Moonlit Waves candles sold at Dollar Tree because high flames can ignite wax or break glass, posing fire and burn risks.

    Product
    Sure Scents 2-1 Peaceful Stream/Moonlit Waves Candles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0109-2021·2020-12-02

    Eywa Pharma Recalls Levetiracetam Tablets Due to Foreign Tablet Presence

    Eywa Pharma Inc. is recalling 500 mg Levetiracetam tablets because a 1000 mg tablet was found in a 500 mg bottle.

    Product
    Levetiracetam Tablets, USP 500 mg, packaged in 120-count bottle, Rx only, Manufactured by: VKT Pharma Private Limited Srikakulam, India - 532 409, Manufactured for: Eywa Pharma Inc. 2 Research Way, Floor 3 Princeton, NJ 08540, NDC 71930-063-52
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0490-2021·2020-12-02

    FDA Recalls Geistlich Bio-Oss Pen Due to Granule Expulsion Risk

    Geistlich Pharma North America is recalling Geistlich Bio-Oss Pen units because granules may be expelled all at once, posing a risk of tissue injury.

    Product
    Geistlich Bio-Oss Pen 0.25-1mm 0.25g - Product Usage: natural bone mineral for filling of bone defects in maxillofacial surgery, implantology, and periodontology. Product Number: 20115
    Category
    Medical Device
    Distribution
    Distributed nationwide