The Recall Desk

State

North Dakota product recalls

73,218 recalls have nationwide distribution and so reach North Dakota. 2,924 additional recalls listed North Dakota specifically in their distribution scope.

What the numbers show

Total
2,924
Critical
265
Severe
729
Most recent
2026-09-23

Of the 2,924 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 729 (25%) are Severe.

These figures cover only the 2,924 recalls whose distribution notice names North Dakota specifically. The 73,218 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

15376–15400 of 76142

  • HighNHTSA·23V540000·2023-08-02

    2022-2023 Nova Bus LFS Transit Buses Battery Short Circuit Fire Risk

    Nova Bus is recalling certain 2022-2023 LFS transit buses because the high-voltage battery may develop a short circuit due to over-tightened rivnut inserts, creating a fire risk.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2242-2023·2023-08-02

    Hernia repair mesh balloon may not inflate during surgery

    Davol Ventralight ST hernia repair mesh balloons may fail to inflate during surgery, potentially causing inadequate mesh placement, infection, and procedure delays.

    Product
    Ventralight ST 4.5" Circle with Echo PS- A low profile, bioresorbable, coated, permanent mesh, with a pre-attached removable positioning system, designed for the reconstruction of soft tissue deficiencies during laparoscopic ventral hernia repair. Catalog Number: 5955450
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V541000·2023-08-02

    Hino Recalls 2022-2023 Trucks for Headlight Installation Defect

    Hino is recalling 468 trucks because improperly installed headlight parts may cause failure or misalignment, increasing crash risk.

    Product
    HINO — HINO NJ7A, NE7A, NJ7B, NV7A
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2227-2023·2023-08-02

    Flexible Laryngeal Mask Airway Packs Lack Required Expiration Date Labels

    Medline Industries is recalling 9,945 DYND3000xxP Series laryngeal mask airway packs because the case and packet labels are missing expiration dates. Without this information, users cannot determine product validity.

    Product
    DYND3000xxP Series - Flexible Laryngeal Mask Airway Packs
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0936-2023·2023-08-02

    Oxacillin for Injection recalled nationwide due to sterility concerns

    Sagent Pharmaceuticals is recalling Oxacillin for Injection USP due to lack of sterility assurance. The recall affects multiple lots distributed nationwide.

    Product
    Oxacillin for Injection, USP, 2 grams per vial, For IV or IM Use, Rx only, labeled as a) NDC 25021-162-24 and b) novaplus NDC 25021-162-68, Mfd. for SAGENT Pharmaceuticals, Schaumburg, IL 60195. Made in India.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2239-2023·2023-08-02

    Argon Medical Option Elite Vena Cava Filter Recall Due to Performance Risk

    Argon Medical Devices is recalling 3 Option Elite Retrievable Vena Cava Filters due to a potential performance defect that could result in pulmonary embolism. Affected units were distributed in Texas.

    Product
    Argon Medical Devices, REF 352506070E, Option Elite Retrievable Vena Cava Filter, Suitable of Jugular or Femoral Delivery, STERILEO, RxOnly, CE 2797
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2234-2023·2023-08-02

    Laser fiber medical devices recalled for potential burn injury hazard

    Boston Scientific recalls Flexiva Pulse laser fibers due to manufacturing defects that can cause fiber connector overheating and potential burns if touched. Affects 280 units in US and Canada.

    Product
    Flexiva Pulse ID 242 TracTip single Use Fiber-intended to be used as a device that transmits Ho:YAG laser energy from cleared laser consoles to urological anatomy 5-pack UPN: M006L8406961
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2230-2023·2023-08-02

    Laser Fiber Devices May Overheat and Cause Burns During Use

    Boston Scientific is recalling Flexiva Pulse 242 laser fibers due to manufacturing defects that may cause the fiber connector to overheat and cause burn injuries. The recall affects 1,245 units distributed in the US and Canada.

    Product
    Flexiva Pulse 242 TracTip Single-Use Laser Fibers -intended to be used as a device that transmits Ho:YAG laser energy from cleared laser consoles to urological anatomy. 5-pack UPN: M006L8405961
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0935-2023·2023-08-02

    Oxacillin Injectable Recalled for Failure to Assure Sterility

    Sagent Pharmaceuticals is recalling Oxacillin for Injection (1 gram vials, Lot OXG301) due to lack of assured sterility. Approximately 65,710 vials distributed nationwide are affected.

    Product
    Oxacillin for Injection, USP, 1 gram per vial, For IV or IM Use, Rx only, Mfd. for SAGENT Pharmaceuticals, Schaumburg, IL 60195. Made in India. NDC 25021-146-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2231-2023·2023-08-02

    Flexiva Pulse ID Laser Fiber Recalled for Incorrect Component

    Boston Scientific is recalling Flexiva Pulse ID laser fibers due to an incorrect component that reduces power output and aiming beam brightness. The component can overheat, risking burns to users who touch the fiber connector.

    Product
    Flexiva Pulse ID-intended to be used as a device that transmits Ho:YAG laser energy from cleared laser consoles to urological anatomy Single-pack UPN: M006L8406910
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2243-2023·2023-08-02

    Ventral Hernia Mesh Balloon May Fail to Inflate During Surgery

    A surgical mesh implant used in ventral hernia repair may fail to inflate properly during the procedure, potentially causing inadequate placement and infection risk. The manufacturer is recalling 169 units worldwide.

    Product
    Ventralight ST w Echo PS 4.5" Circle A low profile, bioresorbable, coated, permanent mesh, with a pre-attached removable positioning system, designed for the reconstruction of soft tissue deficiencies during laparoscopic ventral hernia repair. Catalog Number: 5955450G (EU…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0942-2023·2023-08-02

    Safe Tussin DM Cough Suppressant Recalled for Manufacturing Deviation

    Kramer Laboratories is recalling Safe Tussin DM Cough + Chest Congestion due to a manufacturing deviation involving non-food grade lubricant in the mixing vessel. Affected lots 8753, 8753A, and 8659 were distributed nationwide.

    Product
    Safe Tussin DM Cough + Chest Congestion (Dextromethorphan HBr/ Cough Suppressant Guaifenesin/Expectorant), packaged in 4.0 FL OZ(118mL), 2020 Kramer Laboratories, Inc. Bridgewater, NJ 08807
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2225-2023·2023-08-02

    Diagnostic Verification Product May Not Meet Shelf Life Stability Specifications

    Ortho-Clinical Diagnostics is recalling VITROS NT-proBNP II Range Verifiers Lot 0090 because the product may not meet shelf life stability specifications. Used for diagnostic system calibration verification.

    Product
    VITROS Immunodiagnostic Products NT-proBNP II Range Verifiers-For in vitro diagnostic use only. For use in verifying the calibration range of the VITROS ECi/ECiQ/3600 Immunodiagnostic Systems and the VITROS 5600/XT 7600 Integrated Systems when used for the quantitative…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V537000·2023-08-01

    Freightliner M2 Recalled for Driveshaft Breakage Risk

    Daimler Trucks North America is recalling 2023 Freightliner M2 vehicles because driveshafts can break under certain loading conditions, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23E059000·2023-08-01

    SmartPlug Recalls 30A Shore Power Inlets Due to Fire Risk

    SmartPlug Systems is recalling 30A Shore Power Inlets because D-rings may crack, causing electrical arcing and fire.

    Product
    ELECTRICAL SYSTEM recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V535000·2023-07-31

    Autocar Recalls 2023 Xpeditor Vehicles Due to Fuel Hose Defect

    Autocar is recalling 54 model-year 2023 Xpeditor vehicles because damaged fuel filter hoses may leak or disconnect, increasing the risk of engine stall or fire.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V532000·2023-07-31

    Tiffin Recalls 2023 Phaeton Motorhomes Due to Fuel Hose Defect

    Tiffin is recalling 2023 Phaeton motorhomes because damaged fuel filter hoses may leak or disconnect, increasing the risk of engine stall or fire.

    Product
    TIFFIN — TIFFIN PHAETON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V534000·2023-07-31

    2017-2022 Kia Niro vehicles recalled for engine compartment fire risk

    Kia is recalling 2017–2022 Niro and Niro Plug-in Hybrid vehicles because fluid may leak into the hydraulic clutch actuator, causing an engine compartment fire.

    Product
    KIA — KIA NIRO PHEV, NIRO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V531000·2023-07-31

    2023 Kia Sportage vehicles recalled for electric oil pump fire risk

    Kia America is recalling certain 2023 Sportage vehicles due to a defective electric oil pump controller that may overheat and cause a vehicle fire. Dealers will inspect and replace the controller free of charge.

    Product
    KIA — KIA SPORTAGE, SELTOS, SOUL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V536000·2023-07-31

    Rosenbauer Fire Trucks Recalled for Winch Remote Water Ingress Risk

    Rosenbauer America is recalling specific fire trucks because water can enter the winch remote, causing corrosion that may allow the winch to operate unintentionally.

    Product
    ROSENBAUER — ROSENBAUER COMMANDER, COMMERCIAL M2-112, COMMERCIAL F-550, AVENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V533000·2023-07-31

    Farber Specialty Ford Transit Recall for Fuel Hose Leak Risk

    Farber Specialty Vehicles is recalling one 2021 Ford Transit van because a fuel hose may leak gasoline, increasing the risk of fire.

    Product
    FARBER SPECIALTY — FARBER SPECIALTY FORD TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V528000·2023-07-28

    Midway Specialty Vehicles Recalls 2022 Ford Transit Vans Due to Fuel Leak Risk

    Midway Specialty Vehicles is recalling 2022 Ford Transit vans with Cummins Onan generators because a fuel hose may leak gasoline, increasing fire risk.

    Product
    MIDWAY SPECIALTY VEHICLES — MIDWAY SPECIALTY VEHICLES FORD TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide