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.

40251–40275 of 83599

  • SevereFDA (Drugs)·D-0495-2019·2019-02-20

    Tris Pharma Recalls Superpotent Infants' Ibuprofen Suspension

    Tris Pharma is recalling 35,280 bottles of Infants' Ibuprofen due to potential higher-than-labeled ibuprofen concentrations.

    Product
    Infants' Ibuprofen, Concentrated Ibuprofen Oral Suspension, USP, (NSAID), 50 mg per 1.25 mL, Dye Free, Non-staining Berry Flavor, 1 FL OZ (30 mL) bottle, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, UPC 0 50428 39961 3, NDC 50428-1252-4.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0493-2019·2019-02-20

    Tris Pharma Recalls Infants' Ibuprofen Due to Higher Concentration

    Tris Pharma is recalling specific lots of Infants' Ibuprofen because the medication may contain a higher concentration of ibuprofen than labeled.

    Product
    Infants' Ibuprofen, Concentrated Ibuprofen Oral Suspension, USP, (NSAID), 50 mg per 1.25 mL, Dye Free, Non-staining Berry Flavor, 0.5 FL OZ (15 mL) bottle, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, UPC 0 50428 39338 3, NDC 59779-925-23.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0472-2019·2019-02-20

    Promise Pharmacy Recalls Folic Acid Injection Due to Sterility Concerns

    Promise Pharmacy, LLC is recalling Folic Acid Injection, 10 mg/mL, 10mL vials due to a lack of sterility assurance. The affected lots were distributed nationwide.

    Product
    Folic Acid, Injection, 10 mg/mL, 10mL vial, Rx Only, Promise Pharmacy Compounding Specialists 31818 US Hwy 19N, Palm Harbor, FL 34684
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0824-2019·2019-02-20

    Steris ATLAS Loading Car Recalled for Latch Failure Risk

    Steris Corporation is recalling 129 ATLAS Loading Cars because the latch may fail to engage when empty, causing the unit to slide or fall.

    Product
    ATLAS Loading Car
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0882-2019·2019-02-20

    RXBAR Chocolate Chip Bars Recalled for Undeclared Peanut Allergen

    Chicago Bar Company LLC is voluntarily recalling RXBAR Chocolate Chip bars due to undeclared peanut. Consumers should stop eating the product.

    Product
    RXBAR: Chocolate Chip, 1.83oz bars, single bar,, 12-count carton, , 5-count carton,, 4-count carton
    Category
    Food
    Distribution
    43 states
  • HighFDA (Food)·F-0888-2019·2019-02-20

    RXBAR Mixed Berry Bars Recalled for Undeclared Peanut Allergen

    Chicago Bar Company is voluntarily recalling RXBAR Mixed Berry bars due to undeclared peanut. Consumers should stop eating the product and return it to the store.

    Product
    RXBAR: Mixed Berry, single bar, 12-count carton, UPC 57777 00470, 4-count carton
    Category
    Food
    Distribution
    43 states
  • HighFDA (Devices)·Z-0829-2019·2019-02-20

    AtriCure Recalls COBRA FUSION 50 Ablation Systems Due to Thromboembolism Risk

    AtriCure is recalling 1,288 COBRA FUSION 50 Ablation Systems because patients may face an elevated risk of thromboembolism during specific off-pump procedures.

    Product
    COBRA FUSION 50, Ablation System, Catalog # (REF) 700-002
    Category
    Medical Device
    Distribution
    37 states
  • HighFDA (Drugs)·D-0456-2019·2019-02-20

    Promise Pharmacy Recalls IGF-1 LR3 Injections Due to Sterility Concerns

    Promise Pharmacy is recalling 59 vials of IGF-1 LR3 injections because they lack sterility assurance. The affected products were distributed nationwide.

    Product
    IGF-1 LR3, 620 mcg injection, Rx Only, Promise Pharmacy Compounding Specialists 31818 US Hwy 19N, Palm Harbor, FL 34684
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0612-2019·2019-02-20

    Philips CombiDiagnost R90 X-ray System Recalled for Radiation Dose Risk

    Philips is recalling 146 CombiDiagnost R90 X-ray systems because a software defect may cause patients to receive increased radiation doses.

    Product
    Stationary Fluoroscopic X-ray System CombiDiagnost R90, Model 709030 Stationary Fluoroscopic X-ray System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0892-2019·2019-02-20

    RXBAR Pumpkin Spice Bars Recalled for Undeclared Peanut Allergen

    Chicago Bar Company LLC is voluntarily recalling RXBAR Pumpkin Spice bars due to undeclared peanut allergen.

    Product
    RXBAR: Pumpkin Spice, single bar, 12-count carton, 4-count carton, 1.83 oz bars
    Category
    Food
    Distribution
    43 states
  • HighFDA (Food)·F-0891-2019·2019-02-20

    RXBAR Recalls Kids Chocolate Chip Bars Due to Undeclared Peanut

    RXBAR is voluntarily recalling Kids Chocolate Chip bars because they contain undeclared peanut, a major food allergen.

    Product
    KIDS Chocolate Chip, 1.16 oz. bars, single bar, 16-count carton, 5-count carton
    Category
    Food
    Distribution
    43 states
  • HighFDA (Food)·F-0895-2019·2019-02-20

    RXBAR Recalls 12-Bar Variety Packs Due to Undeclared Peanut Allergen

    Chicago Bar Company LLC is voluntarily recalling RXBAR 12-Bar Variety Packs because they contain undeclared peanut, a major food allergen.

    Product
    RXBAR: 12-Bar Variety Pack (Blueberry, Chocolate Sea Salt, Mixed Berry, Peanut Butter, Peanut Butter Chocolate), See Best By Date on individual bars as noted in other 12-bar pack, 1.83 oz. per bar
    Category
    Food
    Distribution
    43 states
  • HighNHTSA·19V112000·2019-02-20

    Porsche Recalls One 2019 Cayenne Turbo for Shock Absorber Defect

    Porsche is recalling one 2019 Cayenne Turbo because shock absorber forks may allow the shock absorbers to loosen, potentially impairing steering.

    Product
    PORSCHE — PORSCHE CAYENNE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0889-2019·2019-02-20

    RXBAR Recalls Apple Cinnamon Raisin Bars Due to Undeclared Peanut

    Chicago Bar Company LLC is voluntarily recalling RXBAR KIDS Apple Cinnamon Raisin bars because they contain undeclared peanut.

    Product
    RXBAR: KIDS Apple Cinnamon Raisin, 1.16oz bars, single bar, 16-count carton, 5-count carton
    Category
    Food
    Distribution
    43 states
  • HighFDA (Food)·F-0880-2019·2019-02-20

    RXBAR Apple Cinnamon Bars Recalled for Undeclared Peanut Allergen

    Chicago Bar Company LLC is voluntarily recalling RXBAR Apple Cinnamon bars due to undeclared peanut. Consumers should check Best By dates and stop eating the product.

    Product
    RXBAR: Apple Cinnamon,1.83oz bars, single bar, 12-count carton,
    Category
    Food
    Distribution
    43 states
  • HighFDA (Devices)·Z-0831-2019·2019-02-20

    AtriCure Recalls COBRA FUSION 150 Ablation System Due to Thromboembolism Risk

    AtriCure is recalling 175 units of the COBRA FUSION 150 Ablation System because patients may face an elevated risk of thromboembolism during specific off-pump procedures.

    Product
    COBRA FUSION 150 Ablation System, Catalog # (REF) 700-001S
    Category
    Medical Device
    Distribution
    37 states
  • HighFDA (Food)·F-0890-2019·2019-02-20

    RXBAR Recalls KIDS Berry Blast Bars Due to Undeclared Peanut Allergen

    Chicago Bar Company LLC is voluntarily recalling KIDS Berry Blast bars because they contain undeclared peanut, a major food allergen.

    Product
    KIDS Berry Blast, 1.16 oz. bars, single bar, 16-count carton, 5-count carton
    Category
    Food
    Distribution
    43 states
  • HighFDA (Drugs)·D-0475-2019·2019-02-20

    Promise Pharmacy Recalls Pyridoxine HCl Injection Due to Sterility Concerns

    Promise Pharmacy, LLC is recalling 8 vials of Pyridoxine HCl Injection due to a lack of sterility assurance. The product was distributed nationwide in the USA.

    Product
    Pyridoxine HCl, 100 mg/mL Injection, 10ml vial, Rx Only, Promise Pharmacy Compounding Specialists 31818 US Hwy 19N, Palm Harbor, FL 34684
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0893-2019·2019-02-20

    RXBAR Recalls 10-Bar Variety Packs for Undeclared Peanut Allergen

    Chicago Bar Company LLC is voluntarily recalling RXBAR 10-Bar Variety Packs because they contain undeclared peanut, a major food allergen.

    Product
    RXBAR: 10-Bar Variety Pack (Blueberry, Chocolate Sea Salt, Coconut Chocolate, Peanut Butter Chocolate), 1.83 oz. per bar
    Category
    Food
    Distribution
    43 states
  • HighFDA (Food)·F-0887-2019·2019-02-20

    RXBAR Mint Chocolate Bars Recalled for Undeclared Peanut Allergen

    Chicago Bar Company LLC is voluntarily recalling RXBAR Mint Chocolate bars due to an undeclared peanut allergen. The recall affects single, 4-count, and 12-count cartons.

    Product
    RXBAR: Mint Chocolate, 1.83 oz. bars, single bar, 12-count carton, 4-count carton
    Category
    Food
    Distribution
    43 states
  • HighFDA (Food)·F-0884-2019·2019-02-20

    RXBAR Coffee Chocolate Bars Recalled for Undeclared Peanut Allergen

    Chicago Bar Company LLC is voluntarily recalling RXBAR Coffee Chocolate bars due to undeclared peanut. Consumers should check Best By dates and stop eating the product.

    Product
    RXBAR: Coffee Chocolate, 1.83oz bars, single bar, , 12-count carton
    Category
    Food
    Distribution
    43 states
  • HighFDA (Food)·F-0878-2019·2019-02-20

    RXBAR Recalls Coconut Chocolate Bars Due to Undeclared Peanut Allergen

    Chicago Bar Company LLC is voluntarily recalling Coconut Chocolate RXBARs because they contain undeclared peanut, a major food allergen.

    Product
    Coconut Chocolate RXBARs , 1.83 oz., single bar, , 12-count carton, 5-count carton, 4-count carton
    Category
    Food
    Distribution
    43 states
  • HighFDA (Food)·F-0896-2019·2019-02-20

    RXBAR Recalls 14-Bar Variety Packs Due to Undeclared Peanut Allergen

    Chicago Bar Company LLC is voluntarily recalling RXBAR 14-Bar Variety Packs because they contain undeclared peanut, a major food allergen.

    Product
    RXBAR: 14-Bar Variety Pack (Chocolate Chip and Chocolate Sea Salt), 1.83 oz. per bar
    Category
    Food
    Distribution
    43 states
  • HighFDA (Food)·F-0894-2019·2019-02-20

    RXBAR Recalls Variety Packs Due to Undeclared Peanut Allergen

    Chicago Bar Company LLC is voluntarily recalling RXBAR variety packs because they contain undeclared peanut, a major food allergen.

    Product
    RXBAR: 12-Bar Variety Pack (Chocolate Sea Salt, Peanut Butter Chocolate), and 16-Bar Variety Pack (Chocolate Sea Salt, Peanut Butter Chocolate), 1.83 oz. per bar
    Category
    Food
    Distribution
    43 states