The Recall Desk

State

New Jersey product recalls

72,913 recalls have nationwide distribution and so reach New Jersey. 9,759 additional recalls listed New Jersey specifically in their distribution scope.

What the numbers show

Total
9,759
Critical
1,249
Severe
2,482
Most recent
2026-09-09

Of the 9,759 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 2,482 (25%) are Severe.

These figures cover only the 9,759 recalls whose distribution notice names New Jersey specifically. The 72,913 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2001–2025 of 82672

  • SevereCPSC·26483·2026-05-14

    Misco Sports Badminton Toy Sets Recalled Due to Battery Ingestion Risk

    Missry Associates is recalling Misco Sports Badminton Toy Sets because the shuttlecocks contain button cell batteries that children can easily access and swallow, potentially causing serious internal injuries or death.

    Product
    Misco Sports Badminton Toy Sets Red/Blue MT2383
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26485·2026-05-14

    Agio Menlo Woven Patio Swings Recalled Due to Fall Hazard Risk

    World Bright International Limited recalls Agio Menlo Woven Patio Swings (Model 1934256) sold at Costco because the swing seat can detach during use, risking serious injury or death. Eight injuries have been reported.

    Product
    Agio Menlo Woven Patio Swings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26481·2026-05-14

    Tiyol Pull String Teething Toys Recalled for Choking Hazard Risk

    Tiyol Pull String Teething Toys sold on Amazon are recalled due to oversized silicone strings that can lodge in the throat, posing a choking hazard. CPSC is aware of 11 choking incidents.

    Product
    Tiyol Pull String Teething Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26494·2026-05-14

    Electric Start Pressure Washers Recalled for Carbon Monoxide Hazard

    Generac and DR Power electric start pressure washers are recalled because the electronic start/stop button can malfunction and self-start the unit, creating a risk of serious injury or death from carbon monoxide poisoning in confined spaces. No injuries have been reported.

    Product
    Electric Start Pressure Washers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V304000·2026-05-14

    GMC and Other Full-Size SUVs with Faulty Front Wheel Hub Bolts

    General Motors is recalling certain 2025–2026 GMC Yukon, Yukon XL, Chevrolet Tahoe, Suburban 1500, and Cadillac Escalade models with 24-inch wheels due to incorrectly installed front wheel hub bolts that may loosen or break, risking loss of vehicle control.

    Product
    GMC — GMC, CHEVROLET, CADILLAC YUKON, SUBURBAN 1500, TAHOE, ESCALADE ESV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V307000·2026-05-14

    Hyundai Recalls Elantra Vehicles Due to Air Bag Inflator Rupture Risk

    Hyundai is recalling 2015-2016 Elantra and 2016 Elantra GT vehicles because the driver's air bag inflator may rupture during deployment, posing a risk of injury from metal fragments.

    Product
    HYUNDAI — HYUNDAI ELANTRA GT, ELANTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26480·2026-05-14

    Superbobi Pool Drain Covers Recalled for Entrapment and Drowning Risk

    Superbobi 7 3/8-inch pool drain covers violate federal safety standards and pose entrapment and drowning hazards. Pool owners should stop using affected covers immediately.

    Product
    Superbobi 7 3/8 Inch Pool Drain Covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V308000·2026-05-14

    Hyundai Elantra Hybrid power control units may overheat

    Hyundai is recalling certain 2024-2026 Elantra Hybrid vehicles because the hybrid power control unit assembly may overheat, increasing the risk of a fire. 54,337 vehicles are affected.

    Product
    HYUNDAI — HYUNDAI ELANTRA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26489·2026-05-14

    Electric Water Kettles Recalled Due to Burn Hazard from Loosening Handle

    ZWILLING J.A. Henckels has recalled approximately 113,440 ENFINIGY electric kettles in the U.S. because the handle can loosen and separate, causing hot water to spill and posing a burn injury risk.

    Product
    Electric Kettles (ENFINIGY 1.5 l and ENFINIGY Pro 1.5 l)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26487·2026-05-14

    Petzl Climbing and Adventure-Park Harnesses Recalled for Fall-Hazard Risk

    Petzl America is recalling about 1,270 SIMBA and SWAN EASYFIT harnesses because missing rivets in the buckles can cause them to open, creating a risk of serious injury or death from falls.

    Product
    Petzl SIMBA CLIMBING and SIMBA PARK Children's Harnesses, SWAN EASYFIT STEEL and SWAN EASYFIT STAINLESS Harnesses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26488·2026-05-14

    Petzl America Recalls Three Climbing Harness Models for Fall Hazard

    Petzl America is recalling about 29,300 climbing harnesses because the D-ring attachment point can release, creating a risk of serious injury or death from a fall.

    Product
    Petzl ASTRO BOD FAST, ASTRO SIT FAST and CANYON GUIDE harnesses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26484·2026-05-14

    LiCB CR2032 Lithium Coin Batteries Recalled for Child-Resistant Packaging Violation

    Guangzhou Lichengbei Battery Technology Co., Ltd. (LiCB) has recalled about 94,000 CR2032 3V lithium coin batteries sold on Amazon because they lack required child-resistant packaging and warning labels. Ingestion can cause serious internal injuries, chemical burns, and death.

    Product
    LiCB CR2032 3V Lithium Coin Batteries
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V306000·2026-05-14

    Honda Prologue and Acura ZDX rearview cameras may display distorted images

    Honda is recalling certain 2024-2025 Prologue and 2024 Acura ZDX vehicles because the rearview camera screen may display a distorted or blank image. 59,887 vehicles are affected.

    Product
    ACURA — ACURA, HONDA ZDX, PROLOGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·26486·2026-05-14

    Amazon Basics 55 Lbs. Adjustable Dumbbells Recalled for Impact Hazard

    Amazon is recalling Amazon Basics 55 Lbs. Adjustable Dumbbells because weight plates can fail to engage completely and dislodge during use, posing an impact hazard. No injuries have been reported.

    Product
    Amazon Basics 55 Lbs. Adjustable Dumbbells
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1934-2026·2026-05-13

    Cook Centimeter Sizing Catheter recall due to marker band cracking

    Cook Incorporated is recalling Centimeter Sizing Catheters because marker bands may crack or break, potentially causing device fragmentation, vessel injury, or life-threatening harm.

    Product
    Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20 GPN G11916 Catheters for use in angiographic procedures are available in a variety of French sizes, endhole sizes, lengths, materials and designs (e.g., polyethylene or nylon, non-braided or braided with 1:1 torque)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1935-2026·2026-05-13

    Aurous Centimeter Sizing Catheter Recalled for Marker Band Cracking Risk

    Cook Incorporated is recalling Aurous Centimeter Sizing Catheters due to risk of marker band cracking or breakage during angiographic procedures. Potential complications include device fragmentation, vessel injury, and in worst-case scenarios, life-threatening harm or death.

    Product
    Aurous Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20-01 GPN G47308 Sizing catheters are single-use, sterile catheters with gold marker bands. These catheters are for use in angiographic procedures and available in a variety of lengths (70 and 100 cm) and tip co
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0540-2026·2026-05-13

    Lactated Ringers Injection Recalled for Particulate Matter Contamination

    B. Braun Medical Inc. is recalling Lactated Ringer's Injection USP (1000 mL containers) due to the presence of particulate matter. The recall affects 95,412 containers distributed nationwide.

    Product
    LACTATED RINGERS — LACTATED RINGERS (SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2097-2026·2026-05-13

    Medline Convenience Kits recalled for potential sterilization issues

    Medline Industries is recalling multiple convenience kit models due to calibration issues with equipment used to sterilize and package the devices, which could affect sterility assurance levels.

    Product
    See RES for full list. Medline Convenience Kits: 1) CHP COCHLEAR SUPPLEMENT CDS, Model Number: CDS983069G; 2) CHP COCHLEAR SUPPLEMENT CDS, Model Number: CDS983069I; 3) HEAD & NECK CDS-LF, Model Number: CDS983782C; 4) BAPTIST FLOYD BRONCHOSCOPY, Model Number: DYKE1456D; 5) BRONCH
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0519-2026·2026-05-13

    Octreotide Acetate Injectable Suspension Recalled Due to Sterility Assurance

    Teva Pharmaceuticals USA, Inc. is recalling 2,200 kits of Octreotide Acetate for Injectable Suspension (30 mg) due to quality system deficiencies that affect sterility assurance. The recall affects all lots nationwide.

    Product
    OCTREOTIDE ACETATE — OCTREOTIDE ACETATE (OCTREOTIDE ACETATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V309000·2026-05-13

    Lucid Air rear-wheel drive inverters may fail and cut drive power

    Lucid is recalling certain 2024-2025 Air rear-wheel drive vehicles because the Gen 4 inverter may experience internal friction and become damaged, causing a loss of drive power.

    Product
    LUCID — LUCID AIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0513-2026·2026-05-13

    DELFLEX Peritoneal Dialysis Solution Recall Due to Potential Sterility Issues

    Fresenius Medical Care is recalling DELFLEX Dextrose Peritoneal Dialysis Solution bags due to potential leaks from bag perforations that could compromise sterility. Affected patients should contact their healthcare provider immediately.

    Product
    DELFLEX, Dextrose Peritoneal Dialysis Solution with attached stay-safe Exchange Set for Intraperitoneal Dialysis Only, 2.5% DEX. LM/LC, 2L 5PK, Part Number 054-20222, Fresenius Medical Care North America, 920 Winter Street, Waltham, MA 02451.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0518-2026·2026-05-13

    BD PurPrep Povidone-Iodine Topical Solution Sterility Assurance Recall

    CareFusion 213, LLC is recalling BD PurPrep (povidone-iodine 8.3% with isopropyl alcohol 72.5%) due to lack of assurance of sterility and potential product contamination. Affected lots are distributed nationwide.

    Product
    PURPREP — PURPREP (POVIDONE IODINE AND ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0517-2026·2026-05-13

    PurPrep Povidone-Iodine and Isopropyl Alcohol Solution Recalled for Sterility Assurance

    CareFusion 213, LLC is recalling PurPrep sterile topical solution due to lack of assurance of sterility and potential product contamination. The affected product is a povidone-iodine and isopropyl alcohol solution distributed nationwide.

    Product
    PURPREP — PURPREP (POVIDONE IODINE AND ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2062-2026·2026-05-13

    ERBEFLO CleverCap CO2 Tubing and Cap Sets for Endoscopes

    Erbe Medical is recalling ERBEFLO CleverCap CO2 hybrid tubing and cap sets used with endoscopes because the distal connector may allow unintended water flow, potentially leading to water aspiration and serious respiratory complications.

    Product
    ERBEFLO CleverCap CO2: Hybrid CO2 Tubing/Cap Set for Olympus Scopes & CO2 Sources, REF: 20325-239; Hybrid CO2 Tubing/Cap Set for Olympus Scopes & UCR, REF: 20325-240; Hybrid CO2 Tubing/Cap Set for Olympus Scopes, REF: 20325-206; Hybrid CO2 Tubing/Cap Set for Pentax Scopes, REF: 2
    Category
    Medical Device
    Distribution
    Distributed nationwide