The Recall Desk

State

North Dakota product recalls

20,082 recalls have nationwide distribution and so reach North Dakota. 0 additional recalls listed North Dakota specifically in their distribution scope.

About recalls in North Dakota

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect North Dakota consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

6076–6100 of 20082

  • HighFDA (Food)·F-0470-2025·2025-02-12

    Cake Donut Rings Recalled for Potential Listeria Contamination

    FGF, LLC is recalling cake donut rings due to potential contamination with Listeria monocytogenes. Distribution included nationwide US and Canada.

    Product
    item 8201779 GEN PLN CAKE DONUT RINGS PFD 90x2.5 OZ, NET WT 12.66LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1091-2025·2025-02-12

    Philips Azurion and Allura System Patient Tables: Finger Entrapment Risk

    Philips Azurion and Allura system patient tables may trap fingers between the guiding rails and tabletop during manual repositioning, risking finger injury to operators and service personnel.

    Product
    Azurion 7 B12 System Code: (1) 722067 (2) 722225 (3) 722235
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0527-2025·2025-02-12

    FGF LLC Bavarian Bismark pastry items recalled for potential listeria contamination

    FGF LLC is recalling Bavarian Bismark pastry item 8201936 due to potential listeria monocytogenes contamination. The recall covers all product within expiration produced on or before December 13, 2024, distributed nationwide in the US and Canada.

    Product
    item 8201936 NATURAL & ARTIFICIAL FLAVORED BAVARIAN BISMARK, NET WT 13.16 LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0489-2025·2025-02-12

    FGF Yeast Ring Donuts Recalled for Potential Listeria Contamination

    FGF, LLC is recalling over 2 million cases of yeast ring donuts distributed nationwide and in Canada due to potential Listeria monocytogenes contamination. Consumers should not consume the product.

    Product
    item 8201839 PBX YST RING DONUT PFD 108x2.12OZ, NET WT 12.88 LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1046-2025·2025-02-12

    X-Ray Imaging System May Continue Exposure Beyond Safety Limit

    GE Medical Systems' Optima XR646 HD X-Ray imaging systems may allow continued radiation exposure beyond the safety limit without operator confirmation. A warning message displays but does not prevent the excess exposure.

    Product
    Optima XR646 HD. X-Ray imaging system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0529-2025·2025-02-12

    FGF Vanilla Mini Cake Donut Rings Recalled for Listeria Contamination Risk

    FGF, LLC is recalling 2,017,614 cases of vanilla mini cake donut rings due to potential Listeria monocytogenes contamination. The affected product was produced on or before December 13, 2024, and distributed nationwide in the US and Canada.

    Product
    item 8202891 PLAIN VANILLA MINI CAKE DONUT RING BULK 240X1.25OZ, NET WT 16.88 LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1081-2025·2025-02-12

    Philips AlluraXper FD20 Biplane Patient Table Finger Entrapment Risk

    Philips AlluraXper FD20 Biplane patient tables may cause finger entrapment between the tabletop and guiding rails during manual repositioning, affecting operators and service personnel.

    Product
    AlluraXper FD20 Biplane System Code: (1) 722008 (2) 722013
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0219-2025·2025-02-12

    Hydralazine Hydrochloride Tablets Recalled Due to Impurities and Degradation

    SKY Packaging recalls Hydralazine Hydrochloride 25 mg tablets nationwide due to failed quality specifications for impurities and degradation.

    Product
    HydrALAZINE Hydrochloride, 25 mg, 100 Unit Dose Tablets (10x10), USP, Rx only, Manufactured by Strides Pharma Science Ltd, Bengaluru, India, Distributed by McKesson by: McKesson Corporation dba SKY Packaging, TN 38141. NDC 63739-327-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0218-2025·2025-02-12

    Prescription injection recalled for failed stability test results

    Teva Pharmaceuticals is recalling Granix injection due to failed stability test results showing one peptide did not meet specification limits.

    Product
    GRANIX — GRANIX (TBO-FILGRASTIM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0459-2025·2025-02-12

    Monkey Spit Atomic Mop BBQ Sauce recalled for undeclared milk allergen

    Monkey Spit Atomic Mop BBQ Sauce contains undeclared milk from butter, posing a risk to consumers with milk allergies. Affected bottles were distributed primarily to local markets and nationwide through online sales.

    Product
    Monkey Spit "Atomic Mop" BBQ Sauce, 12 fl oz (355ml) glass bottle, 12 bottles/case; Refrigerate after opening; Manufactured by Smith House MFG. 146-A S. Thompson Ave. Nipomo, CA 93444 (805) 619-7959; UPC#8 54540 00212 9
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0484-2025·2025-02-12

    Cheese Paczki Recalled Due to Potential Listeria Monocytogenes Contamination

    FGF, LLC is recalling cheese paczki products nationwide due to potential contamination with listeria monocytogenes. Affected products were produced on or before December 13, 2024.

    Product
    item 8201816 NATURALLY AND ARTIFICIALLY FLAVORED CHEESE PACZKI 66x4OZ, NET WT 14.85 LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0514-2025·2025-02-12

    Sour Cream Cake Donuts Recalled for Potential Listeria Contamination

    FGF, LLC is recalling flavored sour cream cake donuts nationwide due to potential Listeria monocytogenes contamination. Approximately 2.0 million cases distributed in the US and Canada are affected.

    Product
    item 8201886 FLAVOREDSOUR CREAM CAKE DONUT 72x3OZ, NET WT 12.15 LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0519-2025·2025-02-12

    FGF Cake Sticks Recalled for Potential Listeria Contamination

    FGF cake sticks are being recalled nationwide and in Canada due to potential Listeria monocytogenes contamination. Consumers should not eat the product and should return it to retailers.

    Product
    item 8201906 JUST BAKED CAKE STICKS 116x2.9 OZ, NET WT 21.03 LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0488-2025·2025-02-12

    Yeast Ring Donuts Recalled Due to Listeria Contamination Risk

    FGF, LLC is recalling 2,017,614 cases of yeast ring donuts distributed nationwide and in Canada due to potential Listeria monocytogenes contamination. Consumers should not consume the product.

    Product
    item 8201836 GEN YST RING DONUT ZGT PFD 78x3OZ, NET WT 13.16 LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1093-2025·2025-02-12

    Philips Azurion patient tables recalled for finger entrapment risk

    Philips is recalling Azurion 7 M12 and Allura patient tables used in medical imaging systems due to a finger entrapment hazard during manual repositioning. Operators and service personnel may suffer finger injury if fingers are caught between the tabletop and guiding rails.

    Product
    Azurion 7 M12 System Code: (1) 722078 (2) 722223 (3) 722233
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1104-2025·2025-02-12

    Integra Miltex Cryosolutions Cartridges Recalled for Premature Valve Opening

    The Integra Miltex Cryosolutions Cartridges (Model C-CA-23) are being recalled because the valve may open prematurely during assembly, causing the cartridge to empty before use. Approximately 3,352 units were distributed nationwide in the US and Canada.

    Product
    Integra Miltex Cryosolutions Cartridges 4 Pack (23.5g N2O each), Model: C-CA-23, Item: 33517;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1103-2025·2025-02-12

    Nitrous Oxide Cartridges Recalled Due to Premature Valve Opening

    Integra Miltex CryoSolutions N2O cartridges are recalled because the valve may open prematurely, causing partial or complete cartridge emptying before use. Affected units were distributed nationwide and to Canada.

    Product
    Integra Miltex CryoSolutions Cartridges 10 Pack (23.5g N2O each), Model: C-CA-23, Item: 33516;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1112-2025·2025-02-12

    Beckman Coulter Access PCT Reagent Pack Recalled for Calibration Failures

    Beckman Coulter Inc. is recalling specific lots of Access PCT Reagent Pack due to high rates of calibration failures that delay test result reporting on immunoassay systems used in healthcare and laboratory settings.

    Product
    Access PCT Reagent Pack, Catalog Number C53987, when used on Access 2 and UniCel Dxl Immunoassay Systems
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V859000·2025-02-11

    2024 Honda Civic Hatchback: Driver's Seat Fasteners May Not Be Properly Tightened

    Honda and Acura are recalling certain 2023-2024 models including the Civic Hatchback, Accord, and Pilot. The driver's seat frame may not be properly tightened, risking inadequate restraint in a crash.

    Product
    HONDA — 2024 HONDA CIVIC HATCHBACK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V860000·2025-02-11

    2022 Indian FTR1200 Motorcycles Recalled for Fuel Tank Leak Risk

    Indian Motorcycle Company is recalling certain 2022 FTR1200 motorcycles due to fuel tanks with holes that may leak fuel, increasing the risk of fire or injury. Dealers will replace the fuel tank free of charge.

    Product
    INDIAN — 2022 INDIAN FTR1200
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V725000·2025-02-10

    2023-2024 Nissan Z: Loose Fasteners May Prevent Pop-Up Hood Activation

    Certain 2023-2024 Nissan Z vehicles have loose fasteners in the front bumper reinforcement that may prevent the pop-up engine hood from activating, increasing injury risk in frontal pedestrian crashes. Dealers will tighten the fasteners free of charge.

    Product
    NISSAN — 2023 NISSAN Z
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V717000·2025-02-10

    Kenworth W900 and T800 Vehicles Recalled for Unsecured Seat Belt Attachment

    Certain 2018-2024 Kenworth W900 and T800 vehicles may have an additional spacer in the seat belt attachment, causing an unsecured connection. This could prevent the seat belt from properly restraining an occupant during a crash.

    Product
    KENWORTH — 2021 KENWORTH W900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V718000·2025-02-10

    2024 Mazda MAZDA3 and CX-90 Recalled for Camera Display Failure

    Mazda is recalling 2024 MAZDA3 and CX-90 vehicles due to a software error that prevents camera images from displaying, which fails federal rear visibility requirements and increases crash risk.

    Product
    MAZDA — 2024 MAZDA MAZDA3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V720000·2025-02-10

    2022 Toyota Highlander Front Bumper Covers May Detach During Operation

    Toyota is recalling certain 2020-2023 Highlander and Highlander Hybrid vehicles because the front bumper covers may come loose or detach during normal operation, potentially becoming a road hazard.

    Product
    TOYOTA — 2022 TOYOTA HIGHLANDER HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide