The Recall Desk

State

New Jersey product recalls

73,388 recalls have nationwide distribution and so reach New Jersey. 9,769 additional recalls listed New Jersey specifically in their distribution scope.

What the numbers show

Total
9,769
Critical
1,249
Severe
2,939
Most recent
2026-10-07

Of the 9,769 recalls naming New Jersey we have scored against our rubric, 1,249 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,939 (30%) are Severe.

These figures cover only the 9,769 recalls whose distribution notice names New Jersey specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

21601–21625 of 83157

  • HighFDA (Devices)·Z-1679-2022·2022-09-14

    Abbott Alinity m SARS-CoV-2 Control Kit Recalled for Failed Internal Control

    Abbott is recalling 579 kits of its Alinity m SARS-CoV-2 CTRL control kit after reports of failed internal control errors preventing verification of test accuracy.

    Product
    Abbott Alinity m SARS-CoV-2 CTRL Kit, REF 09N78-085, each kit contains 12 x 1.3mL CTRL - and 12 x 1.3 mL CTRL +, For In Vitro Diagnostic Use.
    Category
    Medical Device
    Distribution
    24 states
  • HighFDA (Devices)·Z-1681-2022·2022-09-14

    ChemoLock Infusion Ports Recalled for Unintended Disconnection Risk

    ICU Medical recalls ChemoLock chemotherapy infusion ports for potential unintended disconnection due to spring variation, which may delay therapy and expose patients to caustic substances.

    Product
    Product Description/Item: ChemoLock Bag Spike, 10 units/CL-10-10; ChemoLock BAG SPIKE w/ ADDITIVE PORT, DRY SPIKE/CL-12; APPX 1.5ml,ChemoLock BAG SPIKE WITH ADDITIVE PORT/CL-13; ChemoLock Port/CL2100; ChemoLock Port, 5 Units/CL2100-5; ChemoLock Port/CL2100T; Clave Bag…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1686-2022·2022-09-14

    King's Hawaiian Pretzel Buns Recalled for Potential Bacterial Contamination

    King's Hawaiian pretzel hamburger buns, slider buns, and pretzel bites are recalled nationwide. An ingredient used in manufacturing may contain Cronobacter sakazakii or Clostridium botulinum.

    Product
    King's Hawaiian 10.5 oz. Pretzel Hamburger Buns (UPC 73435000365), 10.2 oz. Pretzel Bites (UPC 73435000525.), and 11 oz. Slider Buns (UPC 73435000372 ) packed in plastic bags. Distributed by King s Hawaiian Bakery West, Inc., 19161 Harborgate Way, Torrance, CA 90501
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1707-2022·2022-09-14

    Piantedosi Frozen Dinner Rolls Recalled for Bacterial Contamination

    Piantedosi Baking Co. is recalling Soft Dinner Roll No Seeds 24-packs due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. The recall affects 18,119 frozen trays distributed across 15 states.

    Product
    Soft Dinner Roll No Seeds Unsliced 24-pack (033474400960)
    Category
    Food
    Distribution
    15 states
  • HighFDA (Drugs)·D-1491-2022·2022-09-14

    Guaifenesin and Dextromethorphan Cough Syrup Recalled for Manufacturing Control Deviations

    Plastikon Healthcare LLC is recalling Guaifenesin and Dextromethorphan cough syrup cups distributed nationwide due to manufacturing processes that were not adequately controlled.

    Product
    GUAIFENESIN AND DEXTROMETHORPHAN 200-20 mg/10 mL, 10 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr. Suite 233, Livonia, MI 48152, NDC 0904-6980-72
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V686000·2022-09-14

    2022 Ford F-150 Parking Light Flickering Defect Recall

    Ford is recalling 2022 F-150 trucks and 2022-2023 Bronco Sport vehicles due to a lighting control module defect causing parking light flickering when headlights are activated. The flickering reduces visibility and increases crash risk.

    Product
    FORD — FORD F-150, BRONCO SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1710-2022·2022-09-14

    Frozen SPR Rolls Recalled for Cronobacter and Botulinum Contamination

    Piantedosi Baking Co. is recalling SPR Roll 12-packs due to potential contamination with Cronobacter sakazakii and Clostridium botulinum bacteria. Affected products were distributed across 15 states.

    Product
    SPR Roll 12-pack (033474501339)
    Category
    Food
    Distribution
    15 states
  • HighFDA (Drugs)·D-1493-2022·2022-09-14

    CORRECTDOSE Children's Pain Relief and Fever Reducer Acetaminophen Recalled for Manufacturing Control Violations

    CORRECTDOSE Children's Fever Reducer (160 mg/5 mL acetaminophen) has been recalled due to manufacturing control deviations. The recall affects 1,464 units distributed nationwide.

    Product
    CORRECTDOSE Children's PAIN RELIEF & Fever Reducer, Cherry, (Acetaminophen 160 mg per 5 mL), 2.04 FL.OZ (60mL), packaged in 12-5mL individual doses, Distributed by Correct Dose Inc, Braintree MA 02184. NDC 62320-311-05 UPC 8 60003 67145 0
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1713-2022·2022-09-14

    Frozen Burger Rolls Recalled for Potential Bacterial Contamination

    Piantedosi Baking Co. is recalling B & W Sweet Burger Roll 12-packs due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. The affected products were distributed across 15 U.S. states.

    Product
    B & W Sweet Burger Roll 12-pack (033474502947)
    Category
    Food
    Distribution
    15 states
  • HighFDA (Drugs)·D-1498-2022·2022-09-14

    Difluprednate Eye Drops Recalled for Defective Container Compromising Sterility

    CIPLA is recalling 3,468 bottles of Difluprednate Ophthalmic Emulsion nationwide due to defective protective caps that could expose the dropper tip and compromise sterility. No injuries have been reported.

    Product
    Difluprednate Ophthalmic Emulsion, 0.05%, 5 mL bottle, RX only, Manufactured for Exelan Pharmecuticals, Inc., Boca Raton, FL 33432, NDC 76282-708-50.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1715-2022·2022-09-14

    Frozen Potato Deli Rolls Recalled for Bacterial Contamination Risk

    Piantedosi Baking Co. recalls Gourmet Potato Deli Rolls due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. Affected frozen products distributed across 15 states; consumers should check lot codes 22081-22115 with March-April 2023 expiration dates.

    Product
    Gourmet Potato Deli Roll 12-pack (033474503647)
    Category
    Food
    Distribution
    15 states
  • HighFDA (Drugs)·D-1495-2022·2022-09-14

    Lidocaine Hydrochloride Jelly Recalled Due to cGMP Deviations and Turbidity

    Akorn, Inc. is recalling 82,689 tubes of Lidocaine Hydrochloride Jelly USP, 2%, due to cGMP deviations and turbidity discovered during sterility testing. The recall affects multiple lots distributed nationwide.

    Product
    Lidocaine Hydrochloride Jelly USP, 2%, Sterile, 30mL tube, Rx only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045, NDC 17478-711-31
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1678-2022·2022-09-14

    External Fixation Wire May Fracture During Surgery, Leaving Fragments in Patient

    OrthoPediatrics Corp is recalling an external fixation wire due to manufacturing variance that may cause the tip to fracture. Fractured fragments could remain in patients.

    Product
    Orthex External Fixation Wire Sharp Bayonet 1.8 x 400 mm Model: K400-18BN
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1486-2022·2022-09-14

    Acetaminophen Oral Solution Recalled for Manufacturing Process Control Failures

    Plastikon Healthcare LLC is recalling acetaminophen oral solution (650 mg per 20.3 mL cup) distributed nationwide due to manufacturing process control failures.

    Product
    Acetaminophen Oral Solution 650 mg / 20.3 mL, 20.3 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr. Suite 233, Livonia, MI 48152, NDC 0904-6820-76
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V687000·2022-09-14

    2022 Volkswagen Taos Engine Stall Software Safety Recall

    Volkswagen is recalling certain 2022 Taos vehicles with all-wheel drive due to engine control unit software that may cause engine stall when coming to a stop, increasing crash risk. Dealers will provide free software updates.

    Product
    VOLKSWAGEN — VOLKSWAGEN TAOS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1709-2022·2022-09-14

    Piantedosi Burger Rolls Recalled for Cronobacter and Botulinum Contamination

    Piantedosi Baking Co. is recalling frozen Gourmet Burger Rolls due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. The recall affects 18,119 units across 15 states.

    Product
    Gourmet Burger Roll 12-pack (033474501322)
    Category
    Food
    Distribution
    15 states
  • HighFDA (Food)·F-1722-2022·2022-09-14

    Brioche-Style Slider Rolls Recalled Due to Bacterial Contamination Risk

    Piantedosi Baking Co. is recalling 18,119 frozen Brioche-Style Slider Roll 24-packs distributed across 15 states due to potential contamination with Cronobacter sakazakii and Clostridium botulinum.

    Product
    Brioche-Style Slider Roll 24-pack (033474512021)
    Category
    Food
    Distribution
    15 states
  • HighFDA (Devices)·Z-1677-2022·2022-09-14

    CARTO VIZIGO Guiding Sheath Recalled Due to Water-Damaged Sterile Packaging

    Biosense Webster is recalling 98 units of CARTO VIZIGO 8.5F guiding sheaths due to water damage to packaging that may have compromised the sterile barrier, creating a potential infection risk.

    Product
    CARTO VIZIGO 8.5F Bi-Directional Guiding Sheath, REF: D138501. Used to introduce various cardiovascular catheters into the heart.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1717-2022·2022-09-14

    Frozen Brioche Burger Rolls Recalled for Bacterial Contamination

    Piantedosi Baking Co. is recalling Brioche Style Burger Rolls (UPC 033474504170) distributed across 15 states due to potential contamination with Cronobacter sakazakii and Clostridium botulinum.

    Product
    Brioche Style Burger Roll 12-pack (033474504170)
    Category
    Food
    Distribution
    15 states
  • HighFDA (Drugs)·D-1490-2022·2022-09-14

    Guaifenesin and dextromethorphan liquid medication recalled for manufacturing control issues

    Plastikon Healthcare LLC is recalling guaifenesin and dextromethorphan liquid medication (280,500 cups) distributed nationwide due to manufacturing control deviations in production.

    Product
    GUAIFENESIN AND DEXTROMETHORPHAN 100 mg-10 mg/5 mL, 5 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr. Suite 233, Livonia, MI 48152. NDC 0904-6844-70
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1492-2022·2022-09-14

    CORRECTDOSE Children's Allergy Relief Recalled Due to Manufacturing Process Control Deviations

    CORRECTDOSE Children's Allergy Relief (Diphenhydramine HCl 12.5 mg per 5 mL) is being recalled nationwide. The FDA determined products were manufactured under conditions with inadequate process control.

    Product
    CORRECTDOSE Children's ALLERGY RELIEF (Diphenhydramine HCl 12.5 mg per 5 mL), 2.04 FL. OZ (60 mL) packaged in 12- 5mL individual doses, Distributed by Correct Dose Inc, Braintree MA 02184. NDC 62320-302-05 UPC 8 60003 67144 3
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1484-2022·2022-09-14

    Acetaminophen Oral Solution 160 mg Recalled for Manufacturing Control Deviations

    Acetaminophen Oral Solution 160 mg/5 mL (290,270 cups) recalled nationwide due to CGMP manufacturing control deviations. Product was distributed to institutional healthcare facilities.

    Product
    Acetaminophen Oral Solution 160 mg / 5 mL, 5 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC 0904-6738-70
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1684-2022·2022-09-14

    Early Bird Bleed Monitoring System Introducer fails to power on

    Saranas, Inc. is recalling 953 units of the Early Bird Bleed Monitoring System Introducer Sheath Set due to a design error that prevents the device from powering on and completing self-tests. The product was distributed nationwide.

    Product
    Early Bird Bleed Monitoring System Introducer Sheath Set, REF: FG001-01 (6F), FG001-02 (8F)
    Category
    Medical Device
    Distribution
    Distributed nationwide