The Recall Desk

State

North Carolina product recalls

72,968 recalls have nationwide distribution and so reach North Carolina. 10,261 additional recalls listed North Carolina specifically in their distribution scope.

What the numbers show

Total
10,261
Critical
1,476
Severe
2,520
Most recent
2026-09-09

Of the 10,261 recalls naming North Carolina we have scored against our rubric, 1,476 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,520 (25%) are Severe.

These figures cover only the 10,261 recalls whose distribution notice names North Carolina specifically. The 72,968 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5226–5250 of 83229

  • HighNHTSA·25E066000·2025-10-10

    Ford Recalls Engine Block Heaters Due to Fire Risk

    Ford is recalling certain engine block heaters for 2023-2026 vehicles because they may overheat and cause a fire. Dealers will replace the heater element and inspect the cord.

    Product
    EQUIPMENT:ELECTRICAL:ENGINE BLOCK HEATER recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V677000·2025-10-09

    Braun Ambulances Recall 2023-2026 Models Due to Cruise Control Defect

    Braun Industries is recalling 2023-2026 ambulances because a damaged brake pedal switch may prevent cruise control from disengaging, increasing crash risk.

    Product
    BRAUN AMBULANCES — BRAUN AMBULANCES LIBERTY TYPE I, EXPRESS PLUS TYPE I, CHIEF XL TYPE I, SELECT CHIEF XL I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26008·2025-10-09

    Portable waist fans recalled after four reports of melting or fire

    About 48,000 Living Glow five-in-one portable waist fans are being recalled because the lithium-ion batteries can overheat while charging; four fans have melted or caught fire.

    Product
    Living Glow portable waist fan
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25E065000·2025-10-09

    Chrysler Recalls Mopar Gear Shift Control Cables Due to Park Function Loss

    Chrysler is recalling specific Mopar Gear Shift Control Cables that may detach from the transmission, preventing the vehicle from shifting into park and increasing the risk of a crash.

    Product
    POWER TRAIN:AUTOMATIC TRANSMISSION:LEVER AND LINKAGE:FLOOR SHIFT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26007·2025-10-09

    Electric pressure cookers recalled after eight reports of severe burn injuries

    About 46,660 Ambiano electric pressure cookers sold at ALDI are being recalled because the lid can be opened before pressure is released; 11 incidents include eight severe burn injuries.

    Product
    Ambiano Electric Pressure Cookers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V676000·2025-10-09

    Nissan and Chevrolet Vans Recalled for Fuel Pump Fuse Short Circuit Risk

    Nissan is recalling 2013-2021 NV200 and 2015-2018 Chevrolet City Express vans because a misrouted sensor harness may damage wires, causing a short circuit that could stall the engine.

    Product
    CHEVROLET — CHEVROLET, NISSAN CITY EXPRESS, NV200 TAXI, NV200, CHEVEROLET SS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V680000·2025-10-09

    Genesis Supreme Recalls One Fifth Wheel Trailer Due to Fire Risk

    Genesis Supreme RV is recalling one 2024 Supreme 28IKS fifth wheel trailer because the air conditioner soft start device may overheat and cause a fire.

    Product
    GENESIS SUPREME — GENESIS SUPREME FIFTH WHEEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2611-2025·2025-10-08

    Reprocessed cardiac mapping catheters recalled over residual particulates on device surfaces

    Medline is recalling 7,913 reprocessed Webster CS 10-electrode catheters because specific lots may carry small residual particulates on patient-contacting surfaces.

    Product
    Reprocessed Webster CS Catheter 10 Electrodes for electrophysiological mapping of cardiac structures. Medline Item Numbers BD710DF282CRH BD710DF282RRH BD710FJ282CRH BD710FJ282RRH
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2616-2025·2025-10-08

    Atlan A350 anesthesia workstations recalled after mechanical ventilation failures were reported

    Draeger is recalling 530 Atlan A350 anesthesia workstations that either indicated a piston ventilator failure before use or suffered a mechanical ventilation failure during use.

    Product
    Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500 Software Version: Not applicable Product Description: The Atlan is an anesthesia workstation intended for use in anesthetizing adults, pediatrics, and neonates. The device can be used for mechanical vent
    Category
    Medical Device
    Distribution
    25 states
  • CriticalFDA (Devices)·Z-2657-2025·2025-10-08

    MRI scanner recalled over ice blockage in magnet helium venting system

    A MAGNETOM Connectom.X MRI system is being recalled because an ice blockage in the magnet venting system could prevent helium from escaping during a quench.

    Product
    MAGNETOM Connectom.X. Model Number: 11371480.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2662-2025·2025-10-08

    MAGNETOM Skyra Fit BioMatrix systems recalled over magnet vent ice blockage

    Siemens is recalling 39 MAGNETOM Skyra Fit BioMatrix systems because an ice blockage in the magnet venting system could stop helium escaping during a quench.

    Product
    MAGNETOM Skyra Fit BioMatrix. Model Number: 11516217.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2610-2025·2025-10-08

    Reprocessed steerable electrophysiology catheters recalled over residual particulates on surfaces

    Medline is recalling 7,913 reprocessed Livewire Steerable Electrophysiology Catheters because specific lots may carry small residual particulates on patient-contacting surfaces.

    Product
    Reprocessed Livewire Steerable Electrophysiology Catheter Item Numbers 401575RH 401582RH 401600RH 401603RH 401606RH 401652RH 401653RH 401654RH 401904RH 401905RH 401908RH 401914RH 401915RH 401918RH 401932RH 401933RH 401934RH 401938RH 401939RH 401940RH 401941
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2654-2025·2025-10-08

    Biograph mMR scanners recalled over ice blockage in magnet venting

    Siemens is recalling 27 Biograph mMR systems because an ice blockage in the magnet venting system could stop helium escaping during a quench.

    Product
    Biograph mMR. Model Number: 10433372.
    Category
    Medical Device
    Distribution
    Distributed nationwide