The Recall Desk

State

North Carolina product recalls

72,984 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 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6901–6925 of 83245

  • SevereNHTSA·25V358000·2025-05-29

    Honda motorcycle crankcase bolt can leak oil onto the rear tire

    Honda is recalling certain 2024 XL750 and 2025 CMX1100 and CRF1100 motorcycles because an improperly manufactured crankcase sealing bolt can let the engine leak oil onto the rear tire.

    Product
    HONDA — HONDA CRF1100, CMX1100, XL750
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25304·2025-05-29

    iWALK Magnetic Wireless Power Banks Recalled for Fire and Burn Hazards

    U2O Global is recalling about 27,500 iWALK Magnetic Wireless Power Banks because the lithium-ion batteries can overheat and ignite. The firm has received 15 reports of fires resulting in 10 burn injuries.

    Product
    iWALK Magnetic Wireless Power Banks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25307·2025-05-29

    VFAUOSIT Kitchen Faucets Recalled for Lead Leaching Into Water

    VFAUOSIT kitchen faucets (model 06BNV) sold on Amazon leach lead and other contaminants into water at levels harmful to infants and young children. Consumers should stop using the faucets immediately.

    Product
    VFAUOSIT Kitchen Faucets, model number 06BNV
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25301·2025-05-29

    Minka Vortic Flow Series light fixtures recalled due to impact injury hazard

    Minka Lighting recalls approximately 2,350 Vortic Flow Series light fixtures because the connection component can weaken, allowing the fixture to fall unexpectedly and pose an injury risk. Two partial detachments have been reported, but no falls or injuries have occurred.

    Product
    Minka Vortic Flow Series light fixtures
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25308·2025-05-29

    My First Snowman Toys Recalled for Choking Hazard Risk

    The Step2 Company is recalling My First Snowman toys because the removable top hat can break into small pieces, posing a choking risk to young children. About 30,800 units are affected.

    Product
    My First Snowman Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25306·2025-05-29

    KICIMPRO Kitchen Faucets Recalled Due to Dangerous Lead Exposure

    KICIMPRO kitchen faucets (model KM800-01-06BN) have been recalled because they leach lead into drinking water at levels that can harm infants and young children. About 50,000 units sold on Amazon from January 2024 through May 2025 are affected.

    Product
    KICIMPRO Kitchen Faucets, model number KM800-01-06BN
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25305·2025-05-29

    BASDEHEN Kitchen Faucets Recalled Due to Dangerous Lead Exposure

    BASDEHEN kitchen faucets (model CFDTTH-000-YGH) sold on Amazon leak lead into drinking water at levels that can harm infants and young children's neurological development. About 24,000 units are affected.

    Product
    BASDEHEN Kitchen Faucets, model number CFDTTH-000-YGH
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V356000·2025-05-29

    Cadillac LYRIQ driver display can go blank while the vehicle moves

    General Motors is recalling certain 2023-2024 Cadillac LYRIQ vehicles because the driver video display may go blank while driving, hiding the speedometer, warning lights and rearview camera image.

    Product
    CADILLAC — CADILLAC LYRIQ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·25V355000·2025-05-29

    Jayco fifth wheel labels may list the wrong tire size

    Jayco is recalling certain 2020-2021 North Point fifth wheel travel trailers because the certification labels may have incorrect tire size information, leading owners to fit the wrong tires.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL NORTH POINT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·25V359000·2025-05-29

    2026 Tesla Model Y Windshield Washer Connector Nozzle Blockage Recall

    Tesla is recalling certain 2026 Model Y vehicles because the wiper arm hose connector may block the windshield washer nozzles, preventing washer fluid from reaching the windshield and reducing driver visibility.

    Product
    TESLA — TESLA MODEL Y
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1746-2025·2025-05-28

    Endopath Echelon Vascular White Reload surgical stapler device lockout

    Ethicon Endo-Surgery is recalling the Endopath Echelon Vascular White Reload surgical stapler due to reports of inadvertent instrument lockout during procedures. The lockout prevents cutting and stapling, potentially requiring conversion to open surgery; one patient death has been reported.

    Product
    Endopath Echelon Vascular White Reload for Advanced Placement Tip (35mm, 4 row); Product code VASECR35
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1759-2025·2025-05-28

    Bard Single Intragastric Linton Balloon Tube difficult plastic plug removal

    C.R. Bard Inc is recalling the Bard Single Intragastric Linton Balloon Tube (REF: 0092740) because users may be unable or find it difficult to remove plastic plugs needed to inflate the gastric and esophageal balloons.

    Product
    Bard¿ Single Intragastric Linton Balloon Tube, REF: 0092740
    Category
    Medical Device
    Distribution
    52 states
  • SevereFDA (Drugs)·D-0442-2025·2025-05-28

    Esomeprazole Magnesium Oral Suspension Recalled for Failed Impurity Specifications

    Zydus Pharmaceuticals is recalling Esomeprazole Magnesium 40 mg delayed-release oral suspension because out-of-specification test results were found for unknown degradation products during stability testing.

    Product
    ESOMEPRAZOLE MAGNESIUM — ESOMEPRAZOLE MAGNESIUM (ESOMEPRAZOLE MAGNESIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1756-2025·2025-05-28

    Bard Blakemore Esophageal-Nasogastric Tube difficult balloon inflation

    C.R. Bard is recalling Bard Blakemore Esophageal-Nasogastric Tubes (Adult) because users may find it difficult or impossible to remove the plastic plugs needed to inflate the gastric and esophageal balloons.

    Product
    Bard Blakemore Esophageal-Nasogastric Tube (Adult) REF: 0092100
    Category
    Medical Device
    Distribution
    52 states
  • SevereFDA (Devices)·Z-1758-2025·2025-05-28

    Bard Blakemore Esophageal-Nasogastric Tube Intermediate Balloon Inflation Difficulty

    C.R. Bard Inc is recalling Bard Blakemore Esophageal-Nasogastric Tubes (Intermediate, REF 0092300) due to reports that plastic plugs may be difficult or impossible to remove, preventing proper inflation of the gastric and/or esophageal balloons.

    Product
    Bard¿ Blakemore Esophageal-Nasogastric Tube (Intermediate)REF: 0092300
    Category
    Medical Device
    Distribution
    52 states
  • SevereFDA (Devices)·Z-1757-2025·2025-05-28

    Bard Blakemore Esophageal-Nasogastric Tube Child Difficult Plug Removal

    C.R. Bard is recalling Bard Blakemore Esophageal-Nasogastric Tubes (Child) due to customer complaints that plastic plugs may be difficult or impossible to remove, preventing inflation of the gastric and esophageal balloons.

    Product
    Bard¿ Blakemore Esophageal-Nasogastric Tube (Child) REF: 0092110
    Category
    Medical Device
    Distribution
    52 states
  • SevereFDA (Devices)·Z-1755-2025·2025-05-28

    Bard Minnesota Four Lumen Esophagogastric Tamponade Tube Recalled

    C.R. Bard Inc is recalling the Bard Minnesota Four Lumen Esophagogastric Tamponade Tube (REF:0092220) because users may be unable to or have difficulty removing plastic plugs needed to inflate the gastric and esophageal balloons.

    Product
    Bard Minnesota Four Lumen Esophagogastric Tamponade Tube, REF:0092220 18 Fr. (6mm, 7/32"), 41" Length (104cm) with 8" (20.3cm) Balloon X-Ray Opaque Rubber
    Category
    Medical Device
    Distribution
    52 states
  • SevereUSDA FSIS·018-2025·2025-05-28

    Hormel Recalls Canned Beef Stew Due to Possible Wood Contamination

    Hormel Foods is recalling approximately 256,185 pounds of Dinty Moore Beef Stew due to possible wood contamination. No injuries have been reported.

    Product
    Hormel Foods Corporation — Hormel Foods Corporation Recalls Canned Beef Stew Product Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V353000·2025-05-28

    Peterbilt rear brake piping clearance can cause loss of service brakes

    PACCAR is recalling certain 2024-2026 Peterbilt 367, 548, 567 and 589 trucks because the rear brake piping assembly may have insufficient clearance, which can cause a loss of service brakes or ABS.

    Product
    PETERBILT — PETERBILT 567, 367, 589, 548
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1760-2025·2025-05-28

    Centerline Biomedical IOPS Guidewire 2 Coating Delamination Risk

    Centerline Biomedical is recalling the IOPS Guidewire 2 (Lot 2404-2005) because the coating may delaminate during use, potentially compromising the guidewire's function during catheter placement procedures.

    Product
    Centerline Biomedical IOPS Guidewire 2, REF ATW-2; Sensorized wire used to navigate through vasculature to facilitate placement of a catheter
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Drugs)·D-0441-2025·2025-05-28

    ChloraPrep One-Step Applicators Recalled Due to Compromised Sterile Packaging

    CareFusion 213, LLC is recalling ChloraPrep One-Step applicators nationwide because affected units may have open seals on the packaging, compromising sterility assurance.

    Product
    CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1791-2025·2025-05-28

    SmartPath to Ingenia Elition X MRI Systems Alignment Error Recall

    Philips is recalling SmartPath to Ingenia Elition X MRI systems due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application. The alignment errors could affect image interpretation.

    Product
    Product Name: SmartPath to Ingenia Elition X; Model Numbers: (1) 782118, (2) 782144;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1785-2025·2025-05-28

    True 3D Viewer Model EP-00003 Software Orientation Display Issue Recall

    Echopixel's True 3D Viewer (Model EP-00003) with certain software versions can display ultrasound image orientation incorrectly, potentially leading to misdiagnosis or incorrect surgical planning.

    Product
    True 3D Viewer, Model: EP-00003
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1787-2025·2025-05-28

    Check-Flo Performer Introducer Medical Device Recall Notice

    Cook Incorporated is recalling Check-Flo Performer Introducer devices because some units from affected lots may contain an incorrectly sized introducer sheath.

    Product
    Check=Flo Performer Introducer, 14.0Fr, Reference Part Number(RPN) REF RCFW-14.0-0-38-30-RB, Order Number (GPN) REF G08957,
    Category
    Medical Device
    Distribution
    Distributed nationwide