The Recall Desk

State

North Dakota product recalls

72,969 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 72,969 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5601–5625 of 75890

  • HighFDA (Drugs)·D-0591-2025·2025-08-27

    Sodium bicarbonate injection vials recalled for lack of assurance of sterility

    Hospira 8.4% Sodium Bicarbonate Injection USP, 50 mEq/50 mL, lot LH2671, is recalled nationwide for lack of assurance of sterility. 15,750 vials are affected.

    Product
    SODIUM BICARBONATE — SODIUM BICARBONATE (SODIUM BICARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0590-2025·2025-08-27

    Epinephrine injection vials recalled for lack of assurance of sterility

    Hospira Epinephrine Injection USP, 1 mg/10 mL, lots LY3681, LY4360 and LY4416, is recalled nationwide for lack of assurance of sterility. 49,620 vials are affected.

    Product
    Vial Label: Epinephrine Injection, USP, 1mg/10mL (0.1 mg/mL), Rx only, Distributed by Hospira, Inc., Lake Forest, IL 60045, USA. NDC 0409-4933-05. Case: NDC 0409-4933-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2330-2025·2025-08-27

    Suture retention devices recalled with no reason stated in FDA record

    DRS Vascular is recalling 264 Q-Stop Suture Retention Devices. The FDA enforcement record for this action carries a placeholder in place of a stated reason for the recall.

    Product
    Brand Name: Q-Stop Product Name: Suture Retention Device Model/Catalog Number: QS Software Version: N/A Product Description: The DRS Vascular Q-Stop Suture Retention Appliance is a sterile, single-use, lightweight device made of biocompatible materials that can be easily installe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2335-2025·2025-08-27

    Calcium test slides recalled after calibration failures delayed patient results

    VITROS Chemistry Products Ca Slides, catalog number 145 0261, generations 67 and above, are recalled because calibration failures on VITROS XT systems delay calcium test results. 174,215 units are affected.

    Product
    VITROS Chemistry Products Ca Slides; Catalog Number: 145 0261;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0595-2025·2025-08-27

    Tavaborole topical solution recalled after discoloration found in one lot

    Tavaborole Topical Solution 5%, 10 mL bottles from lot T401968, distributed by Viona Pharmaceuticals, is recalled because of discoloration. 3,960 bottles are affected.

    Product
    TAVABOROLE — TAVABOROLE (TAVABOROLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2337-2025·2025-08-27

    Strep A test kits recalled after shipment to unlicensed purchasing customers

    Clearview Strep A Exact II Dipstick Respiratory Kits are recalled because a classification error in the inventory system sent devices to customers without the required license to buy them. 5 kits are affected.

    Product
    Clearview Strep A Exact II Dipstick Respiratory Kit, CLIA Waived. Catalog Number: 4581225020
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0592-2025·2025-08-27

    Sensodyne Pronamel toothpaste recalled after tube and carton labels were mixed up

    Sensodyne Pronamel Active Shield toothpaste is recalled for a label mix-up: the outer carton reads Fresh Mint while the tube reads Cool Mint/Whitening. The toothpaste inside is Fresh Mint, as the carton states.

    Product
    Sensodyne PRONAMEL (Potassium nitrate 5%, Sodium fluoride 0.25%) Active SHIELD Toothpaste for Sensitive Teeth, Fresh Mint, Net WT 3.4OZ (96.4g) Tube, 6 tubes x 2 inners, per case, Distributed by GSK Consumer Healthcare, Warren, NJ 07059. UPC 3 10158 35691 2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V555000·2025-08-26

    Polestar 3 front bumper may be missing bolts and detach

    Polestar is recalling certain 2025 Polestar 3 vehicles because the hood wing front bumper may be missing bolts, allowing the bumper to detach and become a road hazard.

    Product
    POLESTAR — POLESTAR POLESTAR 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V550000·2025-08-26

    Forest River Riverstone hydraulic brake lines can fail and leak

    Forest River is recalling certain 2018-2026 Riverstone fifth wheel trailers because the steel hydraulic brake lines may fail and leak brake fluid, causing a loss of brake function.

    Product
    FOREST RIVER — FOREST RIVER RIVERSTONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V554000·2025-08-26

    Tiffin Recalls 2025 GT1 Vans Due to Short Rear Seat Belts

    Tiffin Motorhomes is recalling 2025 GT1 Touring vans because rear seat belt buckles may be too short to fasten, increasing injury risk in a crash.

    Product
    TIFFIN — TIFFIN GT1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V552000·2025-08-26

    Ram ProMaster and Dodge Journey rearview cameras may not display properly

    Chrysler is recalling certain 2019-2021 Ram ProMaster and 2019-2020 Dodge Journey vehicles because cracks in the microprocessor may stop the rearview camera image displaying properly.

    Product
    RAM — RAM, DODGE PROMASTER, JOURNEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25E052000·2025-08-26

    Chrysler Recalls Mopar Rearview Camera Modules Due to Image Display Issues

    Chrysler is recalling specific Mopar rearview camera modules because cracks in the microprocessor may prevent the image from displaying properly, increasing crash risk.

    Product
    BACK OVER PREVENTION: SENSING SYSTEM: CAMERA recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V549000·2025-08-25

    2025–2026 Hyundai Tucson and Santa Fe Engine Fastener Recall

    Hyundai is recalling certain 2025–2026 Tucson and Santa Fe vehicles because engine connecting rod bolts may have been improperly tightened, risking loss of drive power, engine damage, oil leaks, and potential fire.

    Product
    HYUNDAI — HYUNDAI SANTA FE, TUCSON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V548000·2025-08-25

    Kia K4 and Sorento connecting rod bolts may be improperly tightened

    Kia is recalling certain 2025 K4 and Sorento vehicles because the connecting rod bolts in the engine may have been improperly tightened, which can cause a loss of drive power.

    Product
    KIA — KIA K4, SORENTO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25E051000·2025-08-25

    Truck Certification Services Recalls Load Carrying Capacity Labels

    Truck Certification Services is recalling specific Load Carrying Capacity labels where weight units may be reversed, potentially leading to vehicle overloading.

    Product
    EQUIPMENT:OTHER:LABELS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25E050000·2025-08-22

    ZF Recalls Steering Columns Due to Improperly Tightened Bolts

    ZF North America is recalling specific steering columns because improperly tightened bolts may cause steering components to separate, increasing the risk of a crash.

    Product
    STEERING:CRITICAL FASTENERS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V539000·2025-08-22

    Entrada trailer wiring fault can lock up the trailer brakes

    Forest River is recalling certain 2024-2026 East to West Entrada recreational vehicles because an incorrectly wired 7-way harness may cause the trailer brakes to lock up when the RV brakes are applied.

    Product
    EAST TO WEST — EAST TO WEST ENTRADA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V542000·2025-08-22

    New Flyer buses may have too few or misplaced emergency exits

    New Flyer is recalling certain 2012-2025 Xcelsior buses that may have been built without enough emergency exits, or with exits in an incorrect location. This fails FMVSS 217.

    Product
    NEW FLYER — NEW FLYER XCELSIOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V546000·2025-08-22

    Ford Mustang water ingress can disable tail and marker lights

    Ford is recalling certain 2024-2025 Mustang and Mustang GTD vehicles because water may enter the body control module and cut communication with the licence plate, side marker and tail lights.

    Product
    FORD — FORD MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide