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.

11201–11225 of 20199

  • HighCPSC·24709·2023-11-09

    Arctic Cat and Tracker Side-by-Side Vehicles Recall Due to Crash Hazard

    Textron Specialized Vehicles is recalling approximately 6,800 Arctic Cat Prowler Pro and Tracker Off Road 800SX side-by-side vehicles from model years 2022 and 2023 because they can roll away while parked on an incline.

    Product
    Model Year 2022 and 2023 Arctic Cat Prowler Pro / Pro Crew and Tracker Off Road 800SX / 800SX Crew Side by Side Recreational Off Highway Vehicles (ROVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24710·2023-11-09

    Magnolia Market Recalls 3-Wick Glass Candles Due to Fire and Laceration Hazards

    Magnolia Market recalled 3-Wick Glass Candles (batch 120122) due to incorrect wax causing excessive flames and glass breakage. 13 incidents reported with minor property damage in 4 cases; no injuries.

    Product
    Magnolia 26 oz. 3-Wick Glass Candles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24022·2023-11-09

    DR Power Tow-Behind Field and Brush Mowers Recalled for Fire and Burn Hazards

    DR Power Equipment and Generac are recalling approximately 2,930 tow-behind field and brush mowers because the exhaust pipe can break from excessive heat, posing fire and burn hazards. The manufacturer has received 14 reports of fires damaging the mowers.

    Product
    Tow-Behind Field & Brush Mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24712·2023-11-09

    Children's Nightgowns Recalled for Flammability Standard Violation

    iMOONZZZ children's nightgowns sold on Amazon fail to meet federal flammability standards for sleepwear, posing a burn hazard to children. About 13,300 units were sold between March and June 2023.

    Product
    Children's Nightgowns
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24711·2023-11-09

    Polaris RANGER XP 1000 Off-Road Vehicles Recalled for Fire and Crash Hazards

    Polaris is recalling about 1,025 Model Year 2023 RANGER XP 1000 NorthStar off-road vehicles because an improperly installed center brake line can cause overheated brakes and reduced braking performance, posing fire and crash hazards.

    Product
    Model Year 2023 RANGER XP 1000 NorthStar and XP 1000 NorthStar Crew Off-Road Vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24024·2023-11-09

    IKEA LETTAN Mirrors Expanded Recall Due to Laceration Hazard

    IKEA is expanding a recall of LETTAN flat mirrors because plastic wall fittings can break and cause the mirror to fall, creating a laceration hazard. No injuries have been reported.

    Product
    IKEA LETTAN Mirrors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V630000·2023-11-09

    2021-2022 Genesis vehicles fuel pump failure increases crash risk

    Hyundai is recalling certain 2021-2022 Genesis G80, GV80, and GV70 vehicles due to potential fuel pump failures that may cause loss of drive power and increase crash risk. Dealers will replace the fuel pump free of charge.

    Product
    GENESIS — 2022 GENESIS GV80
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·24713·2023-11-09

    E-Z-GO and Tracker Electric Vehicles Recalled for Unintended Movement Crash Hazard

    Textron Specialized Vehicles is recalling about 1,660 E-Z-GO ELiTE Express and Tracker OX EV vehicles because internal motor wiring damage can cause the vehicle to move unintentionally, creating a crash hazard. One incident of unexpected movement has been reported but no injuries.

    Product
    Electric Powered E-Z-GO ELiTE Express L6 and EliTE Express S6 PTV and Tracker OX EV vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0312-2024·2023-11-08

    Salad kit recall: Undeclared egg allergen in Wegman's Organics product

    Braga Fresh Foods is recalling Wegman's Organics Sweet Kale Chopped Salad Kit due to undeclared egg allergen. The product was distributed nationwide and may pose a risk to individuals with egg allergies.

    Product
    Wegman's Organics Sweet Kale Chopped Salad Kit, 8oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0211-2024·2023-11-08

    Cosmedent FlexiCup Polishing System Recalled for Crumbling Elastomer Cup

    Cosmedent is recalling the FlexiCup Composite Finishing & Polishing System due to reports that the elastomer cup material is crumbling. Approximately 7,400 packs distributed worldwide are affected.

    Product
    Cosmedent FlexiCup Composite Finishing & Polishing System, Six Pack, Autoclavable Aluminum Oxide Polishing Instrument, Medium (Blue), REF #403-101, Rx.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V573000·2023-11-08

    2023 Ford F-250, F-350, F-450 Rearview Camera May Not Display

    Certain 2023 Ford F-250, F-350, and F-450 trucks with the Pro Trailer Hitch Assist feature may not display the rearview camera image, reducing rear visibility and increasing the risk of a crash.

    Product
    FORD — 2023 FORD F-350 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0078-2024·2023-11-08

    TUMS Antacid Tablets Recalled for Glass Mineral Wool Contamination

    GlaxoSmithKline is recalling TUMS Antacid 1000 mg chewable tablets in Assorted Berries flavor due to glass mineral wool contamination found in some bottles. Product was distributed nationwide.

    Product
    TUMS Antacid, Calcium Carbonate USP 1000 mg, Assorted Berries flavor, Chewable Tablets, packaged in 265-count bottle, Dist. by: GSK CH, Warren, NJ 07059. NDC: 135-0181-05, UPC 3-0766-3072-14-7
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0201-2024·2023-11-08

    RX Modena Clinical Chemistry Analyzer Recalled for Incorrect Rerun Results

    Randox Laboratories is recalling the RX Modena-IVD Clinical Chemistry Analyzer nationwide due to parameter re-run settings that may fail to function correctly when samples are outside the assay range, potentially resulting in incorrect test results.

    Product
    RX Modena-IVD Clinical Chemistry Analyser Catalog Number: RX9000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0077-2024·2023-11-08

    TUMS Antacid 1000 mg Chewable Tablets Recalled for Glass Mineral Wool Contamination

    GlaxoSmithKline recalls TUMS Antacid 1000 mg Assorted Berries chewable tablets (lot HR6A) due to presence of glass mineral wool. The product was distributed nationwide.

    Product
    TUMS Antacid, Calcium Carbonate USP 1000 mg, Assorted Berries flavor, Chewable Tablets, packaged in 12-count roll, Dist. by: GSK CH, Warren, NJ 07059. NDC: 135-0181-03, UPC 3-0766-0746-70-6
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0199-2024·2023-11-08

    RX Daytona Plus Clinical Chemistry Analyzer Rerun Settings Malfunction

    Randox Laboratories is recalling the RX Daytona Plus (without ISE) IVD Clinical Chemistry Analyzer due to a flaw in rerun settings that may cause incorrect test result reporting.

    Product
    RX Daytona Plus (without ISE)- IVD Clinical Chemistry Analyser (1) RX4041, (2) RX4041R (refurbished)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0207-2024·2023-11-08

    Blood Gas Analyzer Software Issue Causes Erroneous Creatinine Results During Startup

    Nova Biomedical Prime Plus Analyzers may report incorrect creatinine levels during the first 2-4 hours after installing a new sensor cartridge. These errors may not be identified by traditional quality control practices.

    Product
    Nova Biomedical Prime Plus Analyzer -Intended to measure certain gases in blood, serum, plasma or pH of blood, serum, and plasma. (1) PN 57400 Stat Profile Prime Plus Analyzer (2) PN 59508 Stat Profile Prime Plus Analyzer, Remanufactured
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0203-2024·2023-11-08

    Coapt Dome Electrode Gen2 System Recalled for Burn Risk

    Coapt LLC is recalling the Dome Electrode Gen2 system due to potential burns or blistering from exposure to sunlight, warm temperatures exceeding 12 hours, or battery damage.

    Product
    Coapt Dome Electrode, Gen2 system, cutaneous electrode
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0083-2024·2023-11-08

    Liothyronine Sodium Tablets Recalled for Failed Impurity and Degradation Specifications

    Sun Pharmaceutical is recalling 7,392 bottles of Liothyronine Sodium Tablets (Lot DND0058A) nationwide due to failed impurity and degradation specifications. Patients should contact their healthcare provider.

    Product
    LIOTHYRONINE SODIUM — LIOTHYRONINE SODIUM (LIOTHYRONINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0195-2024·2023-11-08

    Siemens Cios Alpha X-ray system software defect may cause patient misdiagnosis

    Siemens Cios Alpha (VA30) C-arm X-ray systems have a software issue that may not meet updated DIN and IEC standards. This defect could result in patient misdiagnosis or unnecessary repeat imaging.

    Product
    Siemens Cios Alpha (VA30) mobile fluoroscopic C-arm X-ray System, designed for the surgical environment. 11105200
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0202-2024·2023-11-08

    RX Monaco-IVD Clinical Chemistry Analyzer rerun feature may report incorrect results

    Randox Laboratories is recalling 13 RX Monaco-IVD Clinical Chemistry Analyzers with a rerun feature defect that may report incorrect test results when samples are outside normal assay range. Units were distributed nationwide including Puerto Rico.

    Product
    RX Monaco-IVD Clinical Chemistry Analyser Catalog Number: RX5000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V636000·2023-11-08

    Indian FTR 1200 S Motorcycles Recalled for Coolant Junction Leak Risk

    Indian Motorcycle Company is recalling certain FTR 1200 and FTR 1200 S motorcycles due to a coolant junction that may leak, posing burn and crash risks to riders.

    Product
    INDIAN — 2020 INDIAN FTR 1200 S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0075-2024·2023-11-08

    TUMS Antacid Recalled for Glass Mineral Wool Contamination

    GlaxoSmithKline is recalling TUMS Antacid (1000mg Calcium Carbonate) due to the presence of glass mineral wool. The affected lot (HV6B) was distributed nationwide.

    Product
    TUMS — TUMS (CALCIUM CARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0076-2024·2023-11-08

    TUMS Antacid Tablets Recalled for Glass Mineral Wool Contamination

    TUMS Antacid chewable tablets (Assorted Berries, 1000 mg, lot HR5W) are being recalled nationwide because some bottles contain glass mineral wool. Consumers should stop using affected bottles immediately.

    Product
    TUMS Antacid, Calcium Carbonate USP 1000 mg, Assorted Berries flavor, Chewable Tablets, packaged in 72-count bottles, Dist. by: GSK CH, Warren, NJ 07059. NDC: 135-0181-02, UPC 3-0766-0746-50-8
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0084-2024·2023-11-08

    Liothyronine Sodium Tablets Recalled for Failed Impurity Specifications

    Sun Pharmaceutical is recalling approximately 2,304 bottles of Liothyronine Sodium Tablets, USP, 25 mcg (lot DNC2204A) due to failed impurity and degradation specifications. The affected medication was distributed nationwide.

    Product
    LIOTHYRONINE SODIUM — LIOTHYRONINE SODIUM (LIOTHYRONINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0200-2024·2023-11-08

    RX Imola Clinical Chemistry Analyzer rerun feature may report results incorrectly

    RX Imola-IVD Clinical Chemistry Analyzers may report test results incorrectly when handling out-of-range samples due to improper parameter rerun settings. 35 units nationwide are affected.

    Product
    RX Imola-IVD Clinical Chemistry Analyzer Catalog Number: RX4900. RX4900R (refurbished)
    Category
    Medical Device
    Distribution
    Distributed nationwide