The Recall Desk

State

North Dakota product recalls

73,509 recalls have nationwide distribution and so reach North Dakota. 2,925 additional recalls listed North Dakota specifically in their distribution scope.

What the numbers show

Total
2,925
Critical
265
Severe
869
Most recent
2026-10-14

Of the 2,925 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 869 (30%) are Severe.

Which agencies issued them

These figures cover only the 2,925 recalls whose distribution notice names North Dakota specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23851–23875 of 76434

  • SevereFDA (Drugs)·D-0092-2022·2021-11-10

    Methocarbamol Tablets Mislabeled with Incorrect Strength

    Bryant Ranch Prepack is recalling Methocarbamol 500mg tablets nationwide because the bottles are mislabeled—they actually contain 750mg tablets. The affected lot was distributed in 30-, 60-, and 90-count bottles.

    Product
    Methocarbamol 500mg Tablet, packaged in a) #30 count (NDC 7133517952), b) #60 count (NDC 7133517954), and c) #90 count (NDC 7133517957) bottles, Rx only, Prinston Laboratories, Packaged by Bryant Ranch Prepack Burbank, CA 91504
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0090-2022·2021-11-10

    Lupin Pharmaceuticals Irbesartan/Hydrochlorothiazide Tablets Recalled for Impurity

    Lupin Pharmaceuticals is recalling Irbesartan and Hydrochlorothiazide Tablets USP (300/12.5 mg) in 30-count and 90-count bottles due to detection of the impurity N-nitrosoirbesartan in the active pharmaceutical ingredient.

    Product
    Irbesartan and Hydrochlorothiazide Tablets USP, 300/12.5 mg a) 30 count (NDC 68180-414-06) and b) 90 count (NDC 68180-414-09) bottles, Rx only
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0114-2022·2021-11-10

    Green Giant Fresh Whole Yellow Onions Recalled for Salmonella Risk

    POTANDON PRODUCE LLC is recalling Green Giant Fresh whole yellow onions sold in 2 lb., 3 lb., and 5 lb. bags due to potential Salmonella Oranienburg contamination. The product was distributed in North Dakota and Minnesota.

    Product
    Green Giant Fresh whole YELLOW onions in 2 lbs. flexible mesh bags, (25/2 lb. pkg. per case) - UPC 60580600120-8. Green Giant Fresh whole YELLOW onions in 3 lbs. flexible mesh bags, (16/3 lb. pkg. per case) - UPC 60580600123-9. Green Giant Fresh whole YELLOW onions in 5 lbs.…
    Category
    Food
    Distribution
    2 states
  • SevereNHTSA·21V872000·2021-11-10

    Maserati Vehicles Recall: Fuel Line Sensor Housing May Crack and Leak

    Maserati is recalling certain 2021-2022 model-year vehicles due to a defective fuel line sensor housing that may crack and leak fuel. The leak can cause engine stall or fire, increasing crash risk.

    Product
    MASERATI — MASERATI GHIBLI, QUATTROPORTE, LEVANTE, MC20
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0116-2022·2021-11-10

    Green Giant Fresh Whole Red Onions Recalled for Salmonella

    Green Giant Fresh whole red onions in 2 lb. mesh bags are being recalled due to potential contamination with Salmonella Oranienburg. The affected product was distributed in North Dakota and Minnesota.

    Product
    Green Giant Fresh whole RED onions in 2 lbs. flexible mesh bags, (18/2 lb. pkg per case) - UPC 60580600248-9.
    Category
    Food
    Distribution
    2 states
  • HighNHTSA·21V871000·2021-11-10

    Ram 1500 Recalled for Inoperable Windshield Defrosting System

    Chrysler is recalling 2022 Ram 1500 vehicles because incompatible HVAC systems may render the windshield defrosting and defogging system inoperable, reducing driver visibility.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0191-2022·2021-11-10

    Lisendo 880 Ultrasound Software displays incorrect cardiac valve measurements

    Lisendo 880 Ultrasound Software versions V1.0–V4.1.3 may not display cardiac measurement results correctly for mitral valve assessments, affecting diagnostic accuracy.

    Product
    Lisendo 880 Ultrasound Software Version: V1.0 through V4.1.3
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0195-2022·2021-11-10

    Siemens COVID-19 Diagnostic Assay Recalled for Inadequate Validation Data

    Siemens is recalling Atellica IM SARS-CoV-2 Antigen Assay kits because validation data submitted to the FDA was insufficient to confirm the assay's accuracy for its intended use.

    Product
    Atellica IM SARS-CoV-2 Antigen Assay (100 Test Kit), SMN # 11207861
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0084-2022·2021-11-10

    Hotdog Buns Recalled for Potential Listeria and Salmonella

    Kansas City LLC, operating as Best Harvest Bakeries, is recalling hotdog buns distributed to restaurants across 14 states due to positive environmental samples tested for Listeria and Salmonella species.

    Product
    Hotdog buns, in unlabeled clear plastic bags, 30 or 12 buns per bag.
    Category
    Food
    Distribution
    15 states
  • HighFDA (Devices)·Z-0186-2022·2021-11-10

    Flexor Check-Flo Introducer Sets recalled due to misplaced radiopaque marker band

    Cook Inc. recalls Flexor Check-Flo Introducer Sets where the radiopaque marker band is incorrectly positioned, which may not be discovered until the device is used in a patient under fluoroscopy, increasing procedural time.

    Product
    Flexor Check-Flo Introducer - Raabe Modification, Introducer Set, RPN KCFW-5.0-38-90-RB-RAABE, GPN G13069 The introducer sheath incorporates a hydrophilic coated Flexor shaft with a hemostasis valve and is provided with a dilator.
    Category
    Medical Device
    Distribution
    17 states
  • HighNHTSA·21V874000·2021-11-10

    Audi Recalls A4, A5, S4, S5, RS 5 Models Due to Air Bag Defect

    Audi is recalling specific 2017-2020 models because a cable fault may disable the passenger air bag, increasing injury risk in a crash.

    Product
    AUDI — AUDI A4, A5, RS 5, S5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0078-2022·2021-11-10

    Hamburger Buns Recalled for Potential Listeria and Salmonella Contamination

    Kansas City LLC, doing business as Best Harvest Bakeries, is recalling hamburger buns distributed to restaurants across 14 states due to positive environmental samples for Listeria and Salmonella species.

    Product
    Hamburger buns, customer specified formula, in unlabeled clear plastic bags, 30 or 12 buns per bag.
    Category
    Food
    Distribution
    15 states
  • HighFDA (Food)·F-0083-2022·2021-11-10

    Potato buns recalled due to Listeria and Salmonella detection

    Kansas City LLC., operating as Best Harvest Bakeries, is recalling potato buns distributed to restaurants across 14 states due to positive environmental samples detected for Listeria and Salmonella species.

    Product
    Potato buns, in unlabeled clear plastic bags, 30 or 12 buns per bag.
    Category
    Food
    Distribution
    15 states
  • HighFDA (Devices)·Z-0187-2022·2021-11-10

    COVENA PICC Sleeve Recalled for Unauthorized FDA Marketing

    Queen Comfort Products is recalling the COVENA PICC Sleeve, marketed without FDA clearance. Patients currently using the device should contact their healthcare provider immediately.

    Product
    COVENA PICC Sleeve
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0200-2022·2021-11-10

    Artis zeego X-Ray System Software Error Affects Image Reconstruction

    Siemens Artis zeego fluoroscopic X-ray systems have a software error that incorrectly displays 3D image reconstruction when the patient table is rotated more than 4 degrees, potentially resulting in incorrect patient treatment during image-guided procedures.

    Product
    Artis zeego, Fluoroscopic X-Ray System Models: 10280959,10502505, 10848283 in combination with the following workplace/system application software models: Product/Model #: syngo X Workplace, 10281061 syngo X Workplace, 10281299 syngo X Workplace, 10502522 Syngo Application…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0082-2022·2021-11-10

    Hamburger buns recalled due to Listeria and Salmonella contamination risk

    Kansas City LLC., operating as Best Harvest Bakeries, is recalling hamburger buns distributed to restaurants across 15 states due to positive environmental samples for Listeria and Salmonella species.

    Product
    Hamburger buns, 5" in unlabeled clear plastic bags, 30 or 12 buns per bag.
    Category
    Food
    Distribution
    15 states
  • HighNHTSA·21V870000·2021-11-10

    Ford recalls 2021 Explorer and Lincoln Aviator suspension modules

    Ford is recalling certain 2021 Explorer and Lincoln Aviator vehicles with incorrect rear suspension module components due to a labeling error. The defect may affect vehicle handling, ride height, and braking, increasing crash risk.

    Product
    LINCOLN — LINCOLN, FORD AVIATOR, EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0079-2022·2021-11-10

    Hotdog Buns Recall Due to Potential Listeria and Salmonella Contamination

    Kansas City LLC., DBA Best Harvest Bakeries is recalling hotdog buns distributed to restaurants across 15 US states due to positive environmental samples for Listeria and Salmonella species.

    Product
    Hotdog buns, customer specified formula, in unlabeled clear plastic bags, 30 or 12 buns per bag.
    Category
    Food
    Distribution
    15 states
  • HighCPSC·22017·2021-11-10

    Hart 18-Gauge 2" Brad Nailers Recalled for Involuntary Nail Discharge

    Hart Consumer Products is recalling about 15,700 Hart 18-Gauge 2" Brad Nailers because the contact sensor can malfunction and cause the tool to involuntarily discharge a nail, posing a risk of serious injury.

    Product
    Hart 18-Gauge 2" Brad Nailers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0190-2022·2021-11-10

    Arietta 850 Ultrasound Software Displays Cardiology Measurements Incorrectly

    FujiFilm Arietta 850 ultrasound systems with affected software versions display cardiology measurement results incorrectly. The recall affects 38 units distributed nationwide.

    Product
    Arietta 850 Ultrasound- Software Version: V1.0.0 through V4.1.3
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0081-2022·2021-11-10

    Hamburger buns recalled for potential Listeria and Salmonella contamination

    Kansas City LLC., doing business as Best Harvest Bakeries, is recalling hamburger buns distributed to restaurants across multiple states due to positive environmental samples for Listeria and Salmonella species.

    Product
    Hamburger buns, 4.5" in unlabeled clear plastic bags, 30 or 12 buns per bag.
    Category
    Food
    Distribution
    15 states
  • HighFDA (Devices)·Z-0189-2022·2021-11-10

    Arietta 750 Ultrasound Software Versions Affected by Incorrect Measurement Display

    FujiFilm Healthcare is recalling Arietta 750 Ultrasound Software versions V1.0.0 through V2.1.3 due to measurement display errors in critical cardiology functions that could lead to incorrect clinical diagnoses. The instruction manual also contains an error.

    Product
    Arietta 750 Ultrasound Software Version: V1.0.0 through V2.1.3
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0192-2022·2021-11-10

    Arietta 65 Ultrasound Software: Calculation Error in EROA Diagnostic Measurements

    Arietta 65 Ultrasound systems with software versions 1.0 through 4.0.0 contain a calculation error that produces incorrect measurements of cardiac valve function during diagnostic assessments.

    Product
    Arietta 65 Ultrasound Software Versions: V1.0 through V4.0.0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0196-2022·2021-11-10

    ADVIA Centaur SARS-CoV-2 Antigen Assay Recalled for Insufficient Validation Data

    Siemens Healthcare Diagnostics is recalling 261 ADVIA Centaur SARS-CoV-2 Antigen Assay test kits distributed nationwide because the FDA determined that validation data submitted for emergency authorization was insufficient to confirm the assay's effectiveness.

    Product
    ADVIA Centaur SARS-CoV-2 Antigen Assay (100 Test Kit), SMN # 11207866
    Category
    Medical Device
    Distribution
    Distributed nationwide