The Recall Desk

State

North Carolina product recalls

73,584 recalls have nationwide distribution and so reach North Carolina. 10,299 additional recalls listed North Carolina specifically in their distribution scope.

What the numbers show

Total
10,299
Critical
1,486
Severe
2,899
Most recent
2026-10-21

Of the 10,299 recalls naming North Carolina we have scored against our rubric, 1,486 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,899 (28%) are Severe.

These figures cover only the 10,299 recalls whose distribution notice names North Carolina specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

651–675 of 83883

  • SevereCPSC·26779·2026-09-17

    LANCHEZ Pressure Washers Recalled for Shock and Electrocution Hazards

    LANCHEZ pressure washers are recalled because they lack a ground-fault circuit-interrupter and adequate power cord, posing risks of shock or electrocution.

    Product
    LANCHEZ Pressure Washers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V599000·2026-09-17

    Jaguar Land Rover Recalls Vehicles for DC-DC Converter Defect

    Jaguar Land Rover is recalling specific 2019-2024 models because a DC-DC converter malfunction can cause loss of drive power and lighting, increasing crash risk.

    Product
    LAND ROVER — LAND ROVER, JAGUAR DEFENDER, DISCOVERY, DISCOVERY SPORT, F-PACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26784·2026-09-17

    Sauna360 Recalls Infrared Saunas Due to Fire and Burn Hazards

    Sauna360 is recalling infrared and hybrid saunas because panels can short circuit and overheat, posing fire and burn risks.

    Product
    Infrared Saunas, Hybrid Infrared Saunas and Infrared Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V598000·2026-09-17

    Toyota Recalls 2026 Lexus and Grand Highlander Models for Steering Knuckle Defect

    Toyota is recalling 617 specific 2026 Lexus and Toyota models because front steering knuckles may crack, potentially causing a loss of steering control.

    Product
    TOYOTA — TOYOTA, LEXUS GRAND HIGHLANDER, GRAND HIGHLANDER HYBRID, RX, RX HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26777·2026-09-17

    Hayward Recalls Universal Pool Heaters Due to Carbon Monoxide Risk

    Hayward Industries is recalling 400,000 BTU Universal-HC Series pool heaters because they can produce high levels of carbon monoxide, posing a risk of serious injury or death.

    Product
    400,000 BTU Universal-HC Series Pool Heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26775·2026-09-17

    Esjay Recalls Toddler Busy Board Toys Due to Choking Hazard

    Esjay is recalling toddler busy board toys because red knobs can detach, posing a choking hazard to children under three.

    Product
    Esjay Toddler Busy Board Montessori Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26773·2026-09-17

    Char-Broil Recalls Bistro Pro Electric Grills Due to Electric Shock Risk

    Char-Broil is recalling about 10,605 Bistro Pro Electric Grills because a grounding wire can disconnect, posing an electric shock hazard. No injuries have been reported.

    Product
    Charbroil Bistro Pro Electric Grills
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26782·2026-09-17

    SHEIN Recalls Pull and Chew Montessori Teething Toys Due to Choking Hazard

    SHEIN is recalling Pull & Chew Montessori Teething Toys because the silicone strings violate safety standards and pose a choking risk. No injuries have been reported.

    Product
    Pull & Chew Montessori Teething Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26780·2026-09-17

    Melissa & Doug Recalls Fire Truck Activity Board Toys Due to Choking Hazard

    Melissa & Doug is recalling about 84,000 Lights & Sounds Fire Truck Activity Board toys sold at Target and Amazon because a fire hose port can detach, posing a choking risk.

    Product
    Lights & Sounds Fire Truck Activity Board
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0869-2026·2026-09-16

    B. Braun Recalls Sodium Chloride Injection Due to Particulate Matter

    B. Braun Medical Inc. is recalling 0.9% Sodium Chloride Injection due to the presence of particulate matter, including iron oxide and fibers.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0865-2026·2026-09-16

    American Regent Recalls Epinephrine Vials Due to Particulate Matter

    American Regent, Inc. is recalling 31,935 vials of Epinephrine Injection due to the presence of particulate matter and broken vials.

    Product
    EPINEPHRINE — EPINEPHRINE (EPINEPHRINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V596000·2026-09-16

    Rewaco Recalls Three-Wheeled Motorcycles Due to Rear Shock Absorber Defect

    Rewaco is recalling 106 three-wheeled motorcycles because a rear shock absorber connection may loosen, potentially causing a loss of vehicle control.

    Product
    Rewaco — Rewaco RF1 ST-3 Touring, RF1 GT Touring, PUR3 GT, PUR3 GT Touring
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3133-2026·2026-09-16

    MedicaLyte Liquid Bicarbonate Concentrate Recalled for High Endotoxin Levels

    Nipro Renal Solutions is recalling MedicaLyte Liquid Bicarbonate Concentrate due to high endotoxin levels. The product is used in hemodialysis.

    Product
    MedicaLyte Liquid Bicarbonate Concentrate REF: BC-100 and BC+201
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3136-2026·2026-09-16

    Nipro Citric Complete Liquid Citric Acid Concentrate Recalled for High Endotoxin Levels

    Nipro Renal Solutions is recalling Citric Complete Liquid Citric Acid Concentrate due to high endotoxin levels. The product was distributed in the US and internationally.

    Product
    Citric Complete Liquid Citric Acid Concentrate REF: LC+200-D,LC+201, LC+225(45X)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0850-2026·2026-09-16

    Baxter Recalls Dextrose Injection Bags Due to Stainless Steel Particulate Matter

    Baxter Healthcare is recalling 606 bags of Dextrose Injection, USP, 70% due to the presence of stainless steel particles in the solution.

    Product
    Dextrose Injection, USP, 70 %, 2000 mL bags, Rx Only, Baxter Healthcare Corporation Deerfield, IL, 60016, Made in USA, NDC 00338-0719-06
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3090-2026·2026-09-16

    Given Imaging Recalls Bravo CF Capsule Delivery Devices Due to Attachment Failure

    Given Imaging is recalling Bravo CF capsule delivery devices because they may fail to attach to the esophagus or detach from the device, posing risks of aspiration and perforation.

    Product
    Bravo CF capsule delivery device, 5-pack, Product Number FGS-0635, Bravo CF capsule delivery device, 1-pack, Product Number FGS-0636. Used to attach a pH monitoring capsule to the esophagus.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V597000·2026-09-16

    Rivian Recalls R1S, R1T, and R2 Vehicles for Rear Camera Obstruction

    Rivian is recalling 2022-2027 R1S, 2022-2026 R1T, and 2027 R2 vehicles because a notification may obstruct the rearview camera image, increasing crash risk.

    Product
    RIVIAN — RIVIAN R1S, R1T, R2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3110-2026·2026-09-16

    Lutronic DermaV Laser System Recalled for Potential Patient Burn Risk

    Lutronic Corporation is recalling 1,065 DermaV Laser Systems because using higher fluences at 1064nm with current cryogen parameters may cause sparks or loud noise, potentially resulting in patient burns.

    Product
    Product Name: DermaV Laser System Model/Catalog Number: DermaV Medical laser device that delivers pulsed laser energy at wavelengths of 532 nm and 1064 nm through a fiber-optic handpiece. The system may be configured with an Intelligent Cooling Device (ICD) to provide…
    Category
    Medical Device
    Distribution
    Distributed nationwide