The Recall Desk

State

North Dakota product recalls

73,566 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 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25101–25125 of 76491

  • HighFDA (Devices)·Z-2156-2021·2021-08-04

    Affinity Four Birthing Bed Latch Mechanism Defect Poses Fall Risk

    The latch mechanism on the Lift-Off foot section of certain Affinity Four Birthing Beds may be damaged, potentially causing improper engagement and creating a fall risk for patients. Hill-Rom is recalling approximately 1,096 affected beds.

    Product
    Affinity Four Birthing Bed-used as a birthing bed for women of child bearing age in an LDR (Labor, Delivery, Recovery) or LDRP (Labor, Delivery, Recovery, Postpartum) setting within the acute care Labor and Delivery market Model Numbers: P3700B, P3700C, P3700D, & P3700E
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2162-2021·2021-08-04

    Coaxial Interventional Needles Recalled for Potential Sterilization Defects

    INNOVATIVE TOMOGRAPHY PRODUCT GMBH is recalling Coaxial Interventional Needles distributed in California due to potential sterilization defects. Needles labeled as sterile may not have been adequately sterilized, creating infection risks.

    Product
    Coaxial Interventional Needle, ITP innotom.com, CE 0297, STERILE EO for the following article numbers: Article no. KIM 22/05, Length 50 mm, diameter 22G/0,7 mm; Article no. KIM 22/07,Length 75 mm, diameter 22 G (0.7 mm); Article no. KIM 22/10, Length 100 mm, diameter 22 G…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V607000·2021-08-04

    2021 Volkswagen ID.4 rear seat belt assemblies may not secure child restraints

    Certain 2021 Volkswagen ID.4 vehicles have rear seat belt assemblies without proper automatic locking function, preventing child restraint systems from securing correctly. Dealers will inspect and replace affected assemblies at no cost.

    Product
    VOLKSWAGEN — VOLKSWAGEN ID.4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2154-2021·2021-08-04

    Daily Toric Contact Lenses Recalled for Misaligned Axis Mark

    CooperVision is recalling SOFMED BREATHABLES 1 DAY TORIC contact lenses (Lot W0106167) due to misaligned axis marks that can cause blurred vision. Affected lenses were distributed in the US and internationally.

    Product
    SOFMED BREATHABLES 1 DAY TORIC Power-07.00 -1.75/ 170 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2148-2021·2021-08-04

    Contact Lens Recall: Misaligned Axis Mark May Cause Blurred Vision

    CooperVision is recalling SPECSAVERS UMERE TORIC daily disposable contact lenses with UV blocker due to a manufacturing defect in which misaligned axis marks may cause blurred vision.

    Product
    SPECSAVERS UMERE TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2139-2021·2021-08-04

    GE CARESCAPE PDM monitor SpO2 display freezes during extended use

    GE Healthcare's CARESCAPE PDM-Masimo SpO2 physiological monitor displays can freeze after extended use without power down, preventing real-time oxygen saturation monitoring.

    Product
    CARESCAPE PDM-Masimo SpO2. Physiological data monitor.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2143-2021·2021-08-04

    Contact Lens Recall: Misaligned Axis Mark May Cause Blurred Vision

    CooperVision is recalling CLARITI 1 DAY TORIC contact lenses with misaligned axis marks that may cause blurred vision. The defective lenses were distributed worldwide including multiple U.S. states.

    Product
    CLARITI 1 DAY TORIC Power: -07.50 -0.75/060 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2147-2021·2021-08-04

    CooperVision CLARITI Contact Lenses Recalled for Misaligned Axis Marks

    CooperVision is recalling CLARITI 1 DAY TORIC contact lenses (Lot U0108940) because misaligned axis marks can cause blurred vision in patients.

    Product
    CLARITI 1 DAY TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2145-2021·2021-08-04

    Contact lens recall due to misaligned axis marking

    CooperVision Inc. is recalling FRESH DAY 1 DAY TORIC contact lenses (Lot R0121629) due to misaligned axis marks that may cause blurred vision in wearers.

    Product
    FRESH DAY 1 DAY TORIC Power -07.50 -0.75/060 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0808-2021·2021-08-04

    Del Monte Fresh Cut Golden Sweet Whole Kernel Corn Recall

    Del Monte Foods is recalling Del Monte Fresh Cut Golden Sweet Whole Kernel Corn due to post-process spoilage discovered in some containers during inspection at a distribution center.

    Product
    Del Monte Fresh Cut Golden Sweet Whole Kernel Corn; 15.25 oz. can (24 x 15.25 oz. cans per case) Case UPC  10024000163029 Can UPC - 024000163022 Distributed by Del Monte Foods, Walnut Creek, CA
    Category
    Food
    Distribution
    19 states
  • ModerateFDA (Devices)·Z-2142-2021·2021-08-04

    ThermoScientific Oxoid Antimicrobial Susceptibility Discs Recalled for Out-of-Specification Performance

    Remel Inc. is recalling certain lots of ThermoScientific Oxoid Antimicrobial Susceptibility Discs because they were manufactured out of specification, potentially affecting laboratory test accuracy. The recall involves 327 units distributed nationwide and to Bermuda.

    Product
    ThermoScientific Oxoid Antimicrobial Susceptibility Discs Rx only Made in the United Kingdom
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2152-2021·2021-08-04

    CooperVision CLARITI 1 DAY TORIC contact lenses recalled for axis misalignment

    CooperVision is recalling CLARITI 1 DAY TORIC contact lenses (Lot W0106186) due to misaligned placement of the axis mark, which can cause blurred vision.

    Product
    CLARITI 1 DAY TORIC Power -07.00 -1.25/010 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2153-2021·2021-08-04

    Contact Lens Axis Mark Misalignment Causes Blurred Vision

    CooperVision's FRESH DAY 1 DAY TORIC contact lenses (lot W0106186) are recalled because misaligned axis marks can cause blurred vision. Affected lenses were distributed worldwide, including in the US, France, Brazil, and other countries.

    Product
    FRESH DAY 1 DAY TORIC Power -07.00 -1.25/010 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0869-2021·2021-08-04

    Now Real Food Organic Steel Cut Oats Mislabeled with Wrong Product

    NOW Health Group Inc. is recalling a specific lot of Organic Steel Cut Oats that may contain Organic Beet Sugar instead of the labeled product. Affected consumers should not consume the product.

    Product
    Now Real Food Organic Steel Cut Oats, 2 lb bag, code 6295, UPC 733739062956, packed 8 bags per case; case packaging is for Now Real Food Organic Beet Sugar 3lbs bags
    Category
    Food
    Distribution
    45 states
  • SevereNHTSA·21V601000·2021-08-03

    Fuel hose leak recall in 2021-2022 Kenworth and Peterbilt trucks

    PACCAR is recalling 688 commercial trucks due to a fuel hose leak between the fuel pump and remote fuel filter head that increases fire risk. Free fuel hose replacement is being offered.

    Product
    KENWORTH — KENWORTH, PETERBILT T480, T280, T380, T370
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E070000·2021-08-03

    Bendix Intellipark Electronic Control Unit Software Recall

    Bendix is recalling Intellipark Dash Electronic Control Units that may fail to activate the parking brake, causing vehicles to move unintentionally.

    Product
    PARKING BRAKE:ELECTRICAL:CONTROL MODULE:SOFTWARE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V595000·2021-08-02

    2021 Audi E-Tron: Unsecured glove box may interfere with air bag

    Volkswagen is recalling certain 2021 Audi E-Tron vehicles because the right hinge pin for the glove box cover may not be properly secured, potentially interfering with knee air bag deployment in a crash.

    Product
    AUDI — AUDI E-TRON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V599000·2021-08-02

    Software error may deactivate rear-view display in 2021 INFINITI Q60 vehicles

    A software error may disable the rear-view camera display in 2021 INFINITI Q60 vehicles, reducing rear visibility and increasing crash risk. Nissan will update the software at no cost.

    Product
    INFINITI — INFINITI Q50, QX80, Q60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V596000·2021-08-02

    2022 Mitsubishi Outlander seat belt retractor defect affects child restraints

    Mitsubishi is recalling certain 2022 Outlander vehicles due to seat belt retractors that may deactivate early, preventing child restraint systems from securing properly. Owners should contact MMNA at 1-888-648-7820 for free replacement.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V598000·2021-08-02

    2020 BMW X4 Engine Software Defect Disables Braking Assist

    BMW is recalling multiple 2020-2021 models, including the X4, due to engine management software that may disable braking assist. Owners should contact BMW at 1-800-525-7417 for a free software update.

    Product
    BMW — BMW, TOYOTA 745LE, X4, X3, M340I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V594000·2021-07-30

    Kawasaki Recalls Ninja H2 SX Motorcycles Due to Rear Wheel Lockup Risk

    Kawasaki is recalling 2018-2021 Ninja H2 SX motorcycles because insufficient grease in the rear hub needle-bearing may cause failure, leading to rear wheel lock-up and increased crash risk.

    Product
    KAWASAKI — KAWASAKI NINJA H2 SX, ZX1002A, ZX1002D
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V593000·2021-07-30

    Kawasaki Recalls 2020-2021 Motorcycles Due to Engine Oil Valve Defect

    Kawasaki is recalling certain 2020-2021 motorcycles because an engine oil pressure relief valve may fail, causing a loss of oil pressure and potential engine stall.

    Product
    KAWASAKI — KAWASAKI Z H2, ZX1002L, NINJA H2, ZX1002N
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V590000·2021-07-30

    Airstream Recalls 2022 Interstate 24X RVs Due to Inverter Wiring Fire Risk

    Airstream is recalling 2022 Interstate 24X recreational vehicles because improperly wired inverters may increase the risk of fire. Dealers will install additional wiring and circuit breakers free of charge.

    Product
    AIRSTREAM — AIRSTREAM INTERSTATE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V591000·2021-07-30

    Entegra Coach Motorhomes Recalled for Fuel Rail Sealing Defect

    Entegra Coach is recalling certain 2018-2022 Anthem, Aspire, Insignia, and Reatta XL motorhomes. A faulty sealing washer in the fuel rail assembly may leak, creating a fire risk. Contact Entegra Coach at 1-800-517-9137 for repairs.

    Product
    ENTEGRA — ENTEGRA REATTA XL, INSIGNIA, ASPIRE, ANTHEM
    Category
    Vehicle
    Distribution
    Distributed nationwide