The Recall Desk

State

North Dakota product recalls

20,199 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.

10776–10800 of 20199

  • ModerateFDA (Drugs)·D-0165-2024·2024-01-03

    Amoxicillin oral suspension recalled for temperature storage deviation

    CARDINAL HEALTHCARE is recalling Amoxicillin for Oral Suspension nationwide due to CGMP deviations. Products were exposed to temperatures outside their labeled storage conditions.

    Product
    AMOXICILLIN — AMOXICILLIN (AMOXICILLIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0198-2024·2024-01-03

    Terconazole Vaginal Suppositories Recalled for Temperature Storage Deviation

    Cardinal Healthcare is recalling Terconazole Vaginal Suppositories (batch 1014228A) distributed nationwide because products were exposed to temperatures outside the labeled storage conditions.

    Product
    TERCONAZOLE — TERCONAZOLE (TERCONAZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0182-2024·2024-01-03

    Fluticasone Propionate Nasal Spray Recalled for Temperature Storage Deviation

    Cardinal Healthcare is recalling Fluticasone Propionate Nasal Spray (50MCG per spray) due to CGMP deviations where products were exposed to temperatures outside labeled storage conditions. Nationwide distribution affected.

    Product
    FLUTICASONE PROPIONATE — FLUTICASONE PROPIONATE (FLUTICASONE PROPIONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V060000·2024-01-02

    General Motors Recalls Pickup Trucks with Defective Power Tailgate Latches

    General Motors is recalling certain 2020-2024 Chevrolet Silverado and GMC Sierra pickup trucks due to faulty electronic tailgate switches that may inadvertently unlatch while the vehicle is parked. The defect can allow the tailgate to open while driving, potentially causing cargo loss and creating a road hazard.

    Product
    CHEVROLET — 2020 CHEVROLET SILVERADO 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V061000·2024-01-02

    Motorhome Seat Pedestal Weld Defect Causes Unsafe Seat Separation Risk

    Jayco is recalling certain 2020-2023 Entegra motorhomes because passenger seats may have improperly welded pedestals that can separate and cause the seat to loosen or detach.

    Product
    ENTEGRA — 2022 ENTEGRA CORNERSTONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V065000·2024-01-02

    2023 Hyundai IONIQ 5 and IONIQ 6 driveshaft replacement recall

    Hyundai is recalling 2023 IONIQ 5, IONIQ 6, and Genesis GV60 vehicles for rear driveshafts that may break under load due to improper heat treatment, causing loss of drive power. Dealers will replace the driveshaft free of charge.

    Product
    HYUNDAI — 2023 HYUNDAI IONIQ 5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V064000·2024-01-02

    Multiple Honda and Acura models recalled for defective airbag sensor

    Honda and Acura are recalling 750,114 vehicles from 2020-2022 model years. A defective front passenger seat weight sensor may fail to suppress the airbag, increasing the risk of injury in a crash.

    Product
    HONDA — 2022 HONDA CIVIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V062000·2024-01-02

    Tiffin Allegro Bay motorhomes recalled for battery fire risk

    Tiffin is recalling certain 2022–2024 Allegro Bay motorhomes because batteries may shift during travel, causing electrical arcing and fire risk. Dealers will install new hold-down hardware at no charge.

    Product
    TIFFIN — 2022 TIFFIN ALLEGRO BAY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V078000·2024-01-02

    Proterra Catalyst and ZX5 buses recalled for wiper motor failure

    Proterra is recalling certain 2020–2022 Catalyst and ZX5 buses due to windshield wiper motor failure. Inoperative wipers reduce visibility and increase crash risk.

    Product
    PROTERRA — 2022 PROTERRA CATALYST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V005000·2024-01-01

    ABS Remorques semi-trailers recalled for coupling plate deterioration

    ABS Remorques is recalling 2014-2023 RC, WC, LRC, and LWC semi-trailers due to coupling plate deterioration that may cause king pin failure and trailer detachment. Detached trailers cannot be controlled and may crash or obstruct traffic.

    Product
    ABS REMORQUES — 2018 ABS REMORQUES RC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V030000·2024-01-01

    2021 Harley-Davidson Motorcycles Instrument Cluster May Fail in Cold Weather

    Certain 2021 Harley-Davidson motorcycles may not display the speedometer or neutral indicator at startup in freezing temperatures, creating a crash risk. Owners should contact Harley-Davidson for a free software update.

    Product
    HARLEY-DAVIDSON — 2021 HARLEY-DAVIDSON RH1250S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·24071·2023-12-28

    High-Powered Magnetic Balls Recalled Due to Ingestion Hazard

    A set of 5mm magnetic balls sold online through Walmart.com via Joybuy is being recalled because the magnets are too strong and can cause serious internal injuries or death if swallowed, especially by children.

    Product
    Relax 5mm Science Kit, Large Hematite Magnets Magnetic Stones Building Blocks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·24070·2023-12-28

    Simpson Gas Pressure Washers Recalled for Lithium Battery Burn Hazard

    FNA Group is recalling about 2,930 Simpson Gas Pressure Washers with Electric Start because the lithium battery in the electric start system can overheat and pose a burn hazard. Two reports of battery overheating have been received, but no injuries have been reported.

    Product
    Simpson Gas Pressure Washers with Electric Start
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0622-2024·2023-12-27

    Frozen Salmon Burgers Recalled for Undeclared Sesame and Milk

    Raw Seafoods Inc. is recalling frozen, lightly seasoned salmon burgers nationwide due to undeclared sesame seeds and milk, which pose serious allergic reaction risk to sensitive consumers.

    Product
    Frozen, Lightly Seasoned Salmon Burgers, 28x6oz., 10.5 lbs cases
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0513-2024·2023-12-27

    FDA Recalls Sterile Water and Saline Bottles for Sterility Assurance Issues

    Nurse Assist, LLC is recalling sterile water and saline bottles across multiple brands due to potential lack of sterility assurance. The products could be nonsterile and may cause infection.

    Product
    Sterile Water/Saline: Brand Name: Product Name/Product Code: CARDINAL: 100ML STERILE SALINE BOTTLE/1020, 100ML STERILE SALINE BOTTLE/1022, 100ML STERILE WATER BOTTLE/1024, 100ML STERILE WATER BOTTLE/10000, 100ML STERILE WATER BOTTLE/PT00103419, 100ML STERILE SALINE BOTTLE/PT001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0151-2024·2023-12-27

    TING 2% Miconazole Nitrate Spray Recalled for Benzene Contamination

    Insight Pharmaceuticals recalls TING 2% Miconazole Nitrate Athlete's Foot Spray due to benzene contamination. The recall affects 117,336 cans distributed nationwide and in Puerto Rico.

    Product
    TING 2% Miconazole Nitrate Athlete's Foot Spray Antifungal Spray Powder, NET WT 4.5 oz (128 g) cans, Distributed by: Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company, Tarrytown, NY 10591, UPC 363736532611.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0541-2024·2023-12-27

    AirFit F30 Full Face Mask recalled for magnetic interference with medical implants

    ResMed is recalling the AirFit F30 Full Face Mask because the device contains magnets that can interfere with active medical implants and ferromagnetic objects. The original user guide did not adequately warn about safe distance requirements.

    Product
    AirFit F30 Full Face Mask and User Guide
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0511-2024·2023-12-27

    IV Flush Syringes and Irrigation Solutions Recalled for Sterility Defect

    Nurse Assist, LLC recalls sodium chloride irrigation solutions and IV flush syringes due to potential lack of sterility assurance, which could allow contamination and infections.

    Product
    0.9% Sodium Chloride: Brand Name: Product Name/Product Code: MAC MEDICAL: 10ML FILL SYRINGE/9210; NURSE ASSIST: 3ML IV FLUSH SYRINGE/1203-BP, 5ML IV FLUSH SYRINGE/1205-BP, 10ML IV FLUSH SYRINGE/1210-BP; SOL: 0.9% SODIUM CHLORIDE IV FLUSH SYRINGE/PFF001; HALYARD OWENS MINOR: 0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0159-2024·2023-12-27

    Blistex Tolnaftate antifungal spray powder recalled for benzene contamination

    Blistex Inc is recalling Odor-Eaters brand Tolnaftate 1% antifungal spray powder nationwide due to benzene contamination. The recall affects approximately 243,386 cases distributed in the USA, Canada, and Korea.

    Product
    BLISTEX — BLISTEX (TOLNAFTATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0539-2024·2023-12-27

    AirFit N20 Nasal Mask: Magnetic Interference with Medical Implants

    ResMed AirFit N20 Nasal Masks contain magnets that may interfere with active medical implants and ferromagnetic objects. The FDA classified this as Class I; ResMed is updating safety warnings with required distances.

    Product
    AirFit N20 Nasal Mask and User Guide
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0153-2024·2023-12-27

    FDA Recalls Phenytoin Oral Suspension Due to Content Uniformity Failure

    The FDA recalled Phenytoin Oral Suspension from Major Pharmaceuticals due to failed content uniformity specifications affecting 3,718 units distributed nationwide.

    Product
    Phenytoin Oral Suspension, USP, 100 mg/4 mL, packaged in packaged in 4 mL unit dose cups (NDC 0904-7079-24), 50 per case (NDC 0904-7079-57), Rx only, Major Pharmaceuticals Livonia, MI 48152
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0536-2024·2023-12-27

    ResMed AirFit N10 Nasal Masks Recalled for Magnetic Interference with Medical Implants

    ResMed is recalling AirFit N10 Nasal Masks because magnets in the masks may interfere with active medical implants. Patients with such implants should consult their healthcare provider before using these masks.

    Product
    AirFit N10 Nasal Masks and User Guide
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0538-2024·2023-12-27

    AirTouch F20 Full Face Mask Recalled for Magnetic Interference with Medical Implants

    ResMed recalls 3.8 million AirTouch F20 full face masks with magnets that may interfere with active medical implants. Updated safety warnings regarding safe distances from medical devices are being issued.

    Product
    AirTouch F20 Full Face Mask and User Guide
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0515-2024·2023-12-27

    Sterile Water Syringes recalled for lack of sterility assurance

    Nurse Assist LLC recalls sterile water injection and irrigation syringes for inadequate sterility assurance. Affected products may be nonsterile and could cause infection if used.

    Product
    Sterile Water: Product Name/Product Code: USP STERILE WATER SYRINGE/1030A, SYRINGE PREFILLED 10 ML/6496722, 30CC PREFILLED SYRINGE/6496723, USP STERILE WATER SYRINGE/1030, 10CC PREFILLED SYRINGES/51638, 30CC PREFILLED SYRINGES/52333, 10CC PREFILLED SYRINGES/1010
    Category
    Medical Device
    Distribution
    Distributed nationwide