The Recall Desk

State

North Dakota product recalls

72,820 recalls have nationwide distribution and so reach North Dakota. 2,921 additional recalls listed North Dakota specifically in their distribution scope.

What the numbers show

Total
2,921
Critical
265
Severe
727
Most recent
2026-09-02

Of the 2,921 recalls naming North Dakota we have scored against our rubric, 265 (9%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 727 (25%) are Severe.

These figures cover only the 2,921 recalls whose distribution notice names North Dakota specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

176–200 of 75741

  • HighFDA (Devices)·Z-2963-2026·2026-08-26

    Maquet Critical Care Recalls Y Sensor Modules for Electrical Safety Testing Omission

    Maquet Critical Care AB is recalling nine Y Sensor Modules for the SERVO-U/-N ventilator systems because they did not undergo required electrical safety and functional tests during production.

    Product
    GETINGE Y SENSOR Module, SERVO-U, SERVO-N, Model Number 6693662; part of the SERVO-U/-N continuous ventilator system, for facility use. Maquet Critical Care AB, is a subsidiary of Getinge.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2977-2026·2026-08-26

    Boston Scientific ENROUTE Transcarotid Neuroprotection System Recall for Tip Separation

    Boston Scientific is recalling ENROUTE Transcarotid Neuroprotection Systems due to a potential for arterial sheath tip separation or partial tip separation during use.

    Product
    Boston Scientific ENROUTE Transcarotid Neuroprotection System, Material Number SR-200-NPS; Percutaneous catheter
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2950-2026·2026-08-26

    EndoFLIP System Recall Due to Incorrect Catheter Expiration Flags

    FDA is recalling 327 EndoFLIP Systems because a software error incorrectly flags catheters as expired, making them unavailable for clinical procedures.

    Product
    EndoFLIP System that includes: ENDOFLIP 1 SYSTEM EF-100 05391530810050 10884521809307 REFURBISHED SYSTEM RFG-EF100 ENDOFLIP 1 10884521808096 05391530810166 DL ENDOFLIP 1 10884521786684 Endoscopic measuring system, including catheter components.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2971-2026·2026-08-26

    Paragon 28 Recalls Custom Foot Implant Due to Material Defect

    Paragon 28, Inc. is recalling a custom-made foot implant due to elevated oxygen levels that may reduce material ductility.

    Product
    Custom Made Device Implant 6123 Navicular Cage Small Right Rev A, Model/Catalog Number 6123S R; foot implant
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2951-2026·2026-08-26

    Foundation Medicine Recalls Hamilton Microlab STAR Liquid Handler Software

    Foundation Medicine is recalling 32 Hamilton Microlab STAR Liquid Handler units due to a software issue causing spontaneous closures.

    Product
    Hamilton Microlab STAR Liquid Handler; Protocol Configuration Tool (PCT) v2.0.0. Used to conduct F1CDx and F1LCDx.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0765-2026·2026-08-26

    Shilpa Medicare Recalls Discolored PEMRYDI RTU Injection Vials

    Shilpa Medicare is recalling 9,489 vials of PEMRYDI RTU (pemetrexed disodium) due to reports of green to dark green discoloration in the solution.

    Product
    PEMRYDI RTU — PEMRYDI RTU (PEMETREXED DISODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0774-2026·2026-08-26

    Mylan Recalls Acamprosate Calcium Tablets Due to Dissolution Failure

    Mylan Pharmaceuticals is recalling Acamprosate Calcium tablets that failed to meet dissolution specifications.

    Product
    ACAMPROSATE CALCIUM — ACAMPROSATE CALCIUM (ACAMPROSATE CALCIUM ENTERIC-COATED)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2968-2026·2026-08-26

    Gentherm Medical Recalls Blanketrol II Thermal Regulating Systems

    Gentherm Medical is recalling 182 Blanketrol II Model 222S thermal regulating systems because overheating of the 115V CPU board may cause the device to shut down.

    Product
    Blanketrol II Model 222S; Thermal regulating system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2972-2026·2026-08-26

    Paragon 28 Recalls Custom Foot Implant Due to Material Defect

    Paragon 28, Inc. is recalling a custom-made foot implant due to elevated oxygen levels that may reduce material ductility.

    Product
    Custom Made Device Implant 6123 Navicular Cage Nominal Right Rev A, Model/Catalog Number 6123N R; foot implant
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V550000·2026-08-25

    Ford Recalls 2026 Maverick, F-150, and Bronco Sport for Joint Issues

    Ford is recalling 2026 Maverick, F-150, and Bronco Sport vehicles because improperly tightened joints may lead to detached parts or loss of vehicle control.

    Product
    FORD — FORD MAVERICK, F-150, BRONCO SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V547000·2026-08-25

    Ford Recalls 2024-2026 Mustangs for Wiring Harness Ground Fracture Risk

    Ford is recalling 2024-2026 Mustangs because engine compartment wiring harness ground connections may fracture, potentially causing loss of drive power or essential vehicle functions.

    Product
    FORD — 2025 FORD MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V548000·2026-08-25

    Ford Recalls 2026 Vehicles for Engine Piston Dome Manufacturing Defect

    Ford is recalling 2026 Explorer, Bronco, Bronco Sport, Mustang, and Ranger vehicles because incorrectly manufactured engine piston domes may fail, causing a loss of drive power.

    Product
    FORD — FORD EXPLORER, BRONCO SPORT, BRONCO, RANGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V549000·2026-08-25

    Mitsubishi Recalls Outlander Models for Rearview Camera Software Defect

    Mitsubishi is recalling 2025-2026 Outlander and 2026 Outlander PHEV vehicles because a software error may prevent the rearview camera image from displaying, increasing crash risk.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER PHEV, OUTLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V546000·2026-08-24

    2027 Thomas Built School Buses Recalled for Missing Seat Belt Anchor Plates

    Daimler Trucks North America is recalling 2027 Thomas Built SAF-T-LINER EFX2 and HDX2 school buses because missing connector plates may compromise seat belt anchorages and body joint strength.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX2, SAF-T-LINER HDX2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E060000·2026-08-24

    Rennline Recalls Lower Control Arms Due to Subframe Damage Risk

    Rennline Automotive is recalling 106 lower control arms that may have incorrect dimensions, potentially damaging the subframe and causing loss of steering control.

    Product
    SUSPENSION:FRONT:CONTROL ARM:LOWER ARM recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V544000·2026-08-21

    PACCAR Recalls 2027 Kenworth and Peterbilt Trucks for Seat Heater Fire Risk

    PACCAR is recalling 811 specific 2027 Kenworth and Peterbilt trucks because a missing heat-shrink on the seat ventilation harness may cause a short circuit and fire.

    Product
    PETERBILT — PETERBILT, KENWORTH 589, W990, T880, T680
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V541000·2026-08-21

    Altec Recalls Aerial Devices and Digger Derricks Due to Braking Calibration Issue

    Altec is recalling specific aerial devices and digger derricks because the automatic braking system was not recalibrated after moving the front radar box, increasing crash risk.

    Product
    ALTEC — ALTEC AA SERIES AERIAL DEVICE, AM SERIES AERIAL DEVICE, DIGGER DERRICK, AN SERIES AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26711·2026-08-20

    Modine Recalls Airedale Ventilation Fans in School Heat Pumps Due to Fire Hazard

    Modine is recalling Airedale ventilation fans in specific school heat pumps because water exposure can cause short circuits and fires. No injuries have been reported.

    Product
    Ventilation Fans in ClassMate® DX Cooling and Air Source Heat Pumps and SchoolMate® Water/Ground Source Heat Pumps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V540000·2026-08-20

    Lucid Recalls 2022-2026 Air Vehicles Due to Fire Risk

    Lucid is recalling 2022-2026 Air vehicles because an electrical circuit may overheat, increasing the risk of fire or reduced visibility.

    Product
    LUCID — 2022 LUCID AIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26713·2026-08-20

    JINHEZO LED Tea Lights Recalled for Battery Ingestion Risk

    CPSC recalls JINHEZO Mini Waterproof LED Tea Lights because accessible button batteries pose a serious injury or death risk if swallowed.

    Product
    JINHEZO Mini Waterproof LED Tea Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide