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.

46626–46650 of 83615

  • HighFDA (Food)·F-0106-2018·2017-11-08

    Wegmans Single Cheese Cannoli Recalled for Undeclared Soy Lecithin

    Wegmans is recalling Single Cheese Cannoli because they contain undeclared soy lecithin. Consumers should check their pantries and discard or return the product.

    Product
    Wegmans Single Cheese Cannoli, 2 oz. UPC: 0-77890-17163
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0104-2018·2017-11-08

    Wegmans Cheese Filled Cannoli Recalled for Undeclared Soy Lecithin

    Wegmans is recalling Large Cheese Filled Cannoli products because they contain undeclared soy lecithin. Consumers in six states should stop eating the product.

    Product
    Wegmans Large Cheese Filled Cannoli, 2 Pack, 5 oz UPC: 0-77890-37951 Wegmans Large Cheese Cannoli, 4 Pack, 10 oz UPC: 0-77890-38014
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0086-2018·2017-11-08

    Sid Wainer & Son Dried Chili Peppers Recalled for Undeclared Peanuts

    Sid Wainer & Son is recalling Jansal Valley brand Dried Chili De Arbol Peppers because the product contains undeclared peanuts.

    Product
    Sid Wainer & Son Jansal Valley brand Dried Chili De Arbol Peppers,packaged in a plastic clamshell container 1 ounce size
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0101-2018·2017-11-08

    Wegmans Marshmellow Treat Recalled for Undeclared Soy Lecithin

    Wegmans is recalling Marshmellow Treat sold by the pound because it contains undeclared soy lecithin, a major allergen.

    Product
    Wegmans Marshmellow Treat sold by the pound UPC: 2-08012-00000
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0087-2018·2017-11-08

    Apple Valley Honey Roasted Crunch Recalled for Undeclared Almonds

    First Source, LLC is recalling Apple Valley Honey Roasted Crunch because the product contains undeclared almonds. The recall affects 32 cases distributed in six states.

    Product
    Apple Valley Honey Roasted Crunch, 15 lb. poly bag lined brown cardboard cases for bulk Item number: 5537606 UPC: 0 23637 02018 0
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0062-2018·2017-11-08

    Smiths Medical Recalls CADD Medication Cassette Reservoirs with Incorrect Pressure Plate

    Smiths Medical ASD Inc. is recalling CADD Medication Cassette Reservoirs because some units may have been manufactured with an incorrect pressure plate.

    Product
    CADD(TM) Yellow Medication Cassette Reservoir with clamp and female Luer. Nonvented stopper included., REF 21-7100-24, 100mL, For use with CADD(R) pumps (except CADD-Micro(TM), CADD-MS(R) 3 and CADD-TPN(R) pumps).STERILE EO, Smiths Medical ASD, Inc. For use with CADD(R) pumps…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0146-2018·2017-11-08

    Aunt Beths Cookies Recalled for Undeclared Peanut or Tree Nut Allergens

    Aunt Beths Cookies is voluntarily recalling specific frozen M&M Cookie products sold between January 1, 2017, and September 28, 2017, due to potential undeclared peanut or tree nut allergens.

    Product
    M&M Cookie, 60- 2.5 oz. cookies, frozen
    Category
    Food
    Distribution
    18 states
  • HighFDA (Devices)·Z-0060-2018·2017-11-08

    Smiths Medical Recalls CADD Medication Cassette Reservoirs with Incorrect Pressure Plates

    Smiths Medical is recalling CADD Medication Cassette Reservoirs because some units may have been manufactured with an incorrect pressure plate.

    Product
    CADD(TM) Medication Cassette Reservoir with clamp and female Luer. Nonvented stopper included., 50 mL, For use with CADD(R) pumps (except CADD-Micro(TM), CADD-MS(R) 3 and CADD-TPN(R) pumps)., REF 21-7001-24, STERILE EO, Smiths Medical ASD, Inc. For use with CADD(R) pumps…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0107-2018·2017-11-08

    Wegmans Dark Bulk Penny Choc Coins Recalled for Undeclared Soy

    Wegmans is recalling Dark Bulk Penny Choc Coins sold in the bakery due to undeclared soy lecithin.

    Product
    Wegmans Dark Bulk Penny Choc Coins, Sold in the Bakery Only UPC: 2-08016-00000
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0150-2018·2017-11-08

    Aunt Beths Cookies Recalled for Undeclared Peanut or Tree Nut Allergens

    Aunt Beths Cookies is voluntarily recalling multiple varieties of cookies sold between January 1, 2017, and September 28, 2017, due to potential undeclared peanut or tree nut allergens.

    Product
    Oatmeal Cookie, 60-2.5 oz. cookies, frozen
    Category
    Food
    Distribution
    18 states
  • HighFDA (Food)·F-0103-2018·2017-11-08

    Wegmans Mini Cheese Filled Cannolis Recalled for Undeclared Soy Lecithin

    Wegmans is recalling Mini Cheese Filled Cannolis because they contain undeclared soy lecithin, a potential allergen.

    Product
    Wegmans Mini Cheese Filled Cannolis 4pk,4 oz. UPC: 0-77890-37952 Wegmans Mini Cheese Filled Cannolis 12 pack, 12 oz. UPC: 0-77890-38013
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0145-2018·2017-11-08

    Aunt Beths Cookies Recalled for Undeclared Peanut and Tree Nut Allergens

    Aunt Beths Cookies is voluntarily recalling specific frozen cookie varieties sold between January 1, 2017, and September 28, 2017, due to potential undeclared peanut or tree nut allergens.

    Product
    Chocolate Chip-N-Chunk Cookie, 72- 2 oz. cookies, frozen
    Category
    Food
    Distribution
    18 states
  • ModerateFDA (Devices)·Z-0061-2018·2017-11-08

    Smiths Medical Recalls CADD Medication Cassette Reservoirs with Incorrect Pressure Plate

    Smiths Medical is recalling CADD Medication Cassette Reservoirs that may have been manufactured with an incorrect pressure plate. The recall covers units distributed worldwide.

    Product
    CADD(TM) Medication Cassette Reservoir with clamp and female Luer., Nonvented stopper included., 100 mL, For use with CADD(R) pumps (except CADD-Micro(TM), CADD-MS(R) 3 and CADD-TPN(R) pumps).REF 21-7002-24, STERILE EO, Smiths Medical ASD, Inc. For use with CADD(R) pumps…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0057-2018·2017-11-08

    Precision Dose Recalls Subpotent Carbamazepine Oral Suspension Unit Dose Cups

    Precision Dose Inc. is recalling Carbamazepine Oral Suspension USP unit dose cups because they tested below the required potency specifications.

    Product
    Carbamazepine Oral Suspension USP, 100 mg/5 mL, 5 mL Unit Dose Cups (NDC 68094-301-59), packaged in 10-count cups per tray, 3 trays per case containing a total of 5 mL x 30 Unit Dose Cups per case (NDC 68094-301-62), Rx only, Pkg: Precision Dose, Inc., S. Beloit, IL 61080.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0055-2018·2017-11-08

    AvKARE Recalls Duloxetine Capsules Due to Slightly Elevated Phthalic Acid

    AvKARE is recalling 274 cartons of Duloxetine Delayed-release Capsules 20 mg due to slightly elevated levels of phthalic acid.

    Product
    Duloxetine Delayed-release Capsules USP, 20 mg, 50 Capsules (5 x 10) Unit Dose per carton, unit dose blister UPC 5026828311), Rx only, Manufactured for: AvKARE, Inc., Pulaski, TN 38478, NDC 50268-283-15.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0069-2018·2017-11-08

    Teva Recalls Dutasteride and Tamsulosin HCl Capsules for Dissolution Failures

    Teva Pharmaceuticals is recalling specific lots of Dutasteride and Tamsulosin HCl capsules because they failed dissolution specifications.

    Product
    Dutasteride and Tamsulosin HCl Capsules, 0.5 mg/ 0.4 mg, packaged in a) 30-count bottle (NDC 0591-3771-30), b) 90-count bottle (NDC 0591-3771-19), Rx only, Manufactured by: Actavis Laboratories FL, Inc. Fort Lauderdale, FL 33314 USA; Distributed by: Actavis Pharma, Inc.…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0056-2018·2017-11-08

    Sanofi Recalls Clofarabine Injection Vials Due to Incorrect Package Insert

    Sanofi-Aventis is recalling 422 vials of Clofarabine injection because the authorized generic product was packaged with the incorrect package insert for the brand name product.

    Product
    Clofarabine injection, 20 mg/20 mL, 20 mL Single-Use Vial, Rx only, Mfd by: Teva Pharmachemle, Swensweg 5, Haarlem, The Netherlands; Mfd for: Winthrop U.S., a business of sanofi-aventis U.S. LLC, Bridgewater, NJ 08807; NDC 0955-1746-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·18025·2017-11-07

    Norco Recalls Children's Bicycles Due to Crank Failure Hazard

    Norco Bicycles is recalling specific children's models because the cranksets can bend or break during use, posing a fall hazard.

    Product
    Children's bicycles with Samox cranksets
    Category
    Consumer Product
    Distribution
    Distributed nationwide