The Recall Desk

State

New Jersey product recalls

73,833 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.

These figures cover only the 9,782 recalls whose distribution notice names New Jersey specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

46801–46825 of 83615

  • ModerateUSDA FSIS·110-2017·2017-10-13

    Battistoni Salami and Capocollo Recalled for Aluminum Contamination

    Battistoni Italian Specialty Meats is recalling specific lots of Genoa Salami and Capocollo due to possible aluminum contamination. No illnesses have been reported.

    Product
    Cup and Char Pepperoni, Inc. — Battistoni Italian Specialty Meats, LLC, Recalls Salami and Capocollo Products Due To Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    6 states
  • SevereNHTSA·17V646000·2017-10-12

    West-Mark Recalls 2011 Tanker Trailer Due to Brake Caliper Bolt Issue

    West-Mark is recalling one 2011 tanker trailer because brake caliper bolts may not be properly torqued, which could cause the calipers to detach and result in a loss of braking ability.

    Product
    WEST-MARK — WEST-MARK TANKER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V643000·2017-10-12

    Keystone Recalls 2018 Triple Axle Toy Haulers Due to Suspension Defect

    Keystone RV is recalling 2018 Carbon, Fuzion, and Raptor triple axle toy haulers because an incorrectly welded suspension equalizer may fail, increasing crash risk.

    Product
    KEYSTONE — KEYSTONE RAPTOR, CARBON, FUZION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V642000·2017-10-12

    HME Recalls 2015 Silverfox SFO Fire Trucks Due to Steering Defect

    HME is recalling 2015 Silverfox SFO fire emergency trucks because improperly torqued steer axles may cause the tie rod to loosen, leading to a loss of steering.

    Product
    HME — HME SFO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V647000·2017-10-12

    Polaris Recalls Victory Motorcycles Due to Brake Line Melting Risk

    Polaris is recalling 2010-2017 Victory motorcycles because engine misfires can melt the rear brake line, increasing crash risk.

    Product
    VICTORY — VICTORY MAGNUM, CROSS COUNTRY, CROSS COUNTRY TOUR, CROSS ROADS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3578-2017·2017-10-11

    Garden of Life Baby Organic Liquid Probiotic Recalled for Choking Hazard

    Garden of Life is recalling 8,475 units of Baby Organic Liquid probiotic formula due to a choking hazard for newborns caused by the liquid's thickness.

    Product
    Garden of Life, Baby Organic Liquid probiotic formula, 56 ml (1.9 fl oz)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V641000·2017-10-11

    Caterpillar Recalls 2016 CT660 Trucks for Steering Defect

    Caterpillar is recalling 2016 CT660 trucks because a loose tie rod could cause a complete loss of steering, increasing crash risk.

    Product
    CATERPILLAR — CATERPILLAR CT660
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0002-2018·2017-10-11

    Inopak Recalls Antibacterial Hand Wash Due to Potential Bacterial Contamination

    Inopak Ltd is recalling Option Systems and STYLE Antibacterial Hand Wash due to GMP deviations and potential bacterial contamination from a pump.

    Product
    Option Systems Antibacterial Foaming Hand Wash, 0.3% P.C.M.X., 8 fl oz and 18 fl oz. bottles and 500, mL 800 mL, and 1000 mL pouches, ALSO labeled as STYLE Antibacterial Hand Soap, Inopak Ltd Ringwood, NJ --- NDC 5031-431-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3609-2017·2017-10-11

    Cargill Recalls Shoprite Chocolate Chips for Undeclared Milk

    Cargill is recalling Shoprite Real Semi-Sweet Chocolate Chips due to undeclared milk. The recall affects specific 24-ounce packages sold in six states.

    Product
    Shoprite Real Semi-Sweet Chocolate Chips, Net Wt. 24 oz., UPC 41190-02668 best by dates 4-11-2019 and 4-12-2019.
    Category
    Food
    Distribution
    6 states
  • SevereNHTSA·17V637000·2017-10-11

    Nissan Recalls 2012 Versa Hatchbacks for Front Coil Spring Fracture Risk

    Nissan is recalling 2012 Versa Hatchbacks sold in 23 states and D.C. because road salt may corrode front coil springs, potentially causing them to fracture and puncture tires.

    Product
    NISSAN — NISSAN VERSA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0013-2018·2017-10-11

    Grand Supercenter Recalls Haioreum Rice Pop Snack for Undeclared Wheat

    Grand Supercenter Inc. is recalling Haioreum Rice Pop Snack due to an undeclared wheat allergen. The recall follows a consumer report of an allergic reaction.

    Product
    HAIOREUM, RICE PANCAKE, KOREAN STYLE SNACK 5.29 OZ (150 G), Sweet Potato
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0014-2018·2017-10-11

    Grand Supercenter Recalls Haioreum Rice Pan Cake for Undeclared Wheat

    Grand Supercenter Inc. is recalling Haioreum Rice Pan Cake, Korean Style Snack, Matcha flavor due to undeclared wheat allergen.

    Product
    HAIOREUM, RICE PANCAKE, KOREAN STYLE SNACK 5.29 OZ (150 G), Matcha (Green Tea)
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0009-2018·2017-10-11

    Pro Bioteks Bio-35 Supplement Recalled for Undeclared Soy Lecithin

    Pro Bioteks Laboratories is recalling Bio-35 dietary supplements because they contain undeclared soy lecithin, a common allergen.

    Product
    Bio35, Vitamin-Mineral Omega Oils Trace Minerals Dietary Supplement, 100 Softgel Capsules. UPC 0-26341-12900-2
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0001-2018·2017-10-11

    KIND Dark Chocolate Nuts and Sea Salt Bars Recalled for Undeclared Walnuts

    KIND LLC is recalling Dark Chocolate Nuts and Sea Salt Bars because the outer box fails to declare the allergen walnuts, although individual bars are properly labeled.

    Product
    KIND Dark Chocolate Nuts and Sea Salt Bar-containing 12 /1.4 oz (40 g) bars Box :16.08 oz (480 g) per pack. Box UPC: 02652 17751
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0006-2018·2017-10-11

    Permobil Electric Wheelchair Bases Recalled for Top Plate Assembly Failure

    Permobil is recalling 146 electric wheelchair bases due to a potential failure of the top plate assembly that connects the seating system to the base.

    Product
    Electric Wheelchair bases: a) C300 b) C350 c) C400 d) C500
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0015-2018·2017-10-11

    Grand Supercenter Recalls Haioreum Rice Pan Cake for Undeclared Wheat

    Grand Supercenter Inc. is recalling Haioreum Rice Pan Cake, Korean Style Snack due to an undeclared wheat allergen that caused a consumer allergy reaction.

    Product
    HAIOREUM, RICE PANCAKE, KOREAN STYLE SNACK 5.29 OZ (150 G), Pumpkin
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-0005-2018·2017-10-11

    Permobil Recalls Electric Wheelchairs Due to Top Plate Assembly Failure Risk

    Permobil is recalling 5,539 Corpus II electric wheelchairs because the top plate assembly may fail, potentially disconnecting the seating system from the base.

    Product
    Electric Wheelchairs: a) C300 CORPUS II b) C350 CORPUS II c) C400 CORPUS II d) C400 CORPUS II LR e) C500 CORPUS II f) C500 CORPUS II LR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3237-2017·2017-10-11

    Radiometer AutoCheck5+ Level 2 Quality Control Ampoules Recalled for Inaccurate Results

    Radiometer America is recalling AutoCheck5+ Level 2 quality control ampoules because they may provide incorrect pCO2 and pO2 results.

    Product
    AutoCheck5+, Level 2, specifically designed for Radiometer Americas blood gas analyzers The QUALICHECK+ quality control (QC) ampoules are specifically designed for Radiometer America s blood gas analyzers
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0004-2018·2017-10-11

    Inopak Choice Antibacterial Hand Soap Recalled for Potential Bacterial Contamination

    Inopak Ltd is recalling Choice Antibacterial Hand Soap due to GMP deviations and potential bacterial contamination from a pump.

    Product
    Choice Antibacterial Hand Soap, (ethyl alcohol 61%) 800 ml/ 27 fl oz, Universal Valve, Inopak LTD, Ringwood, NJ
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0007-2018·2017-10-11

    Implant Direct Recalls Swish Duo-Grip Healing Collars Due to Wrong Component

    Implant Direct is recalling 50 units of Swish Duo-Grip Healing Collars because the packages contained the wrong component size.

    Product
    Implant Direct Swish Duo-Grip Healing Collar, Length: 3mm, Platform: 4.8 mm, Rx only, Sterile Dental Implant component.
    Category
    Medical Device
    Distribution
    Distributed nationwide