The Recall Desk

State

North Dakota product recalls

73,363 recalls have nationwide distribution and so reach North Dakota. 2,924 additional recalls listed North Dakota specifically in their distribution scope.

What the numbers show

Total
2,924
Critical
265
Severe
729
Most recent
2026-09-23

Of the 2,924 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 729 (25%) are Severe.

These figures cover only the 2,924 recalls whose distribution notice names North Dakota specifically. The 73,363 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

17376–17400 of 76287

  • ModerateFDA (Devices)·Z-1251-2023·2023-03-22

    BioFire BCID2 Diagnostic Panels Recalled for Temperature-Related Performance Issues

    BioFire Diagnostics is recalling BioFire BCID2 diagnostic panels that experienced temperature excursions during shipment, which may reduce their performance. Affected kits were distributed in Florida and Georgia.

    Product
    In Vitro Diagnostic (IVD) Panel BioFire BCID2 Panel - REF RFIT-ASY-0147
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0462-2023·2023-03-22

    Clobazam tablets recalled for potential manufacturing cross-contamination risk

    Breckenridge Pharmaceuticals is recalling certain lots of Clobazam 10 mg tablets due to a potential cross-contamination risk stemming from manufacturing process deviations.

    Product
    Clobazam Tablets, 10 mg, CIV, 100-count bottle, Rx only, Manufactured by Centaur Pharmaceuticals Pvt. Ltd., Pune, INDIA, Distributed by: Breckenridge Pharmaceuticals, Inc., Berlin, CT 06037, NDC 51991-900-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1252-2023·2023-03-22

    BioFire Respiratory Panel 2.1 Recalled Due to Temperature Shipping Excursions

    BioFire Diagnostics is recalling BioFire Respiratory Panel 2.1 (RP2.1) diagnostic kits due to temperature excursions during shipping that may reduce device performance.

    Product
    In Vitro Diagnostic (IVD) Panel BioFire Respiratory Panel 2.1 (RP2.1) - REF 423742
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1253-2023·2023-03-22

    In Vitro Diagnostic GI Panel Recalled Due to Temperature Exposure During Shipping

    BioFire Diagnostics is recalling FilmArray GI Panel diagnostic kits due to temperature excursions during shipping that may reduce test performance.

    Product
    In Vitro Diagnostic (IVD) Panel FilmArray GI Panel - REF RFIT-ASY-0116
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0609-2023·2023-03-22

    Organic Sunflower Lecithin Powder Recalled for Undeclared Peanut Allergen

    Navada Imports is recalling Organic Sunflower Lecithin Powder (44 lb boxes) due to undeclared peanut allergen. The product was distributed to a distributor in Missouri and then nationwide to manufacturers.

    Product
    Organic Sunflower Lecithin Powder Packaged in 44 lb. (20 kg.) boxes
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0580-2023·2023-03-22

    Two Rivers Coffee pods recalled for undeclared peanut residue

    Two Rivers Coffee hot cocoa pods in variety packs may contain undeclared peanut residue. Consumers with peanut allergies should not consume these products and should check the affected product codes.

    Product
    Cold Stone Creamery Hot Cocoa Peanut Butter Cup Perfection packaged in single serve pods. Pods are packaged in the following Two Rivers Variety Pack boxes: -Two Rivers Coffee Hot Cocoa Pods, Single Serve Variety Sampler Pack , 40 Count UPC: 810683022554 -Two Rivers Coffee Hot…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0466-2023·2023-03-22

    Buprenorphine Transdermal System 20 mcg/hour Recalled for Specification Failure

    AVEVA Drug Delivery Systems recalls Buprenorphine Transdermal System 20 mcg/hour (Lot 51836) nationwide due to degradation product impurity exceeding specification limits during stability testing.

    Product
    Buprenorphine Transdermal System, CIII 20 mcg/hour, 4 Transdermal Systems One package of 4 disposal units, Rx Only, Manufactured by: Aveva Drug Delivery Systems Inc. Miramar, FL. 33025, Manufactured for: Apotex Corp Weston, FL. 33326, NDC 60505-7079-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0464-2023·2023-03-22

    Evamist (Estradiol) Transdermal Spray Recalled for Failed Content Uniformity

    Padagis US LLC is recalling 43,238 cartons of Evamist (Estradiol) transdermal spray nationwide because the spray content uniformity specification for standard deviation was not met at the 18-month stability time point.

    Product
    EVAMIST — EVAMIST (ESTRADIOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0465-2023·2023-03-22

    Buprenorphine Transdermal System Recalled for Failed Impurity Specifications

    AVEVA Drug Delivery Systems recalls nationwide batches of Buprenorphine Transdermal patches due to a degradation impurity exceeding acceptable limits during stability testing.

    Product
    Buprenorphine Transdermal System, CIII 10 mcg/hour, 4 Transdermal Systems One package of 4 disposal units, Rx Only, Manufactured by: Aveva Drug Delivery Systems Inc. Miramar, FL. 33025, Manufactured for: Apotex Corp Weston, FL. 33326, NDC 60505-7077-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·23E022000·2023-03-20

    Meritor Recalls Front Drive Steer Axles Due to Loose Fasteners

    Meritor is recalling specific front drive steer axles because fasteners may not be tightened sufficiently. This defect could cause axle separation and loss of vehicle control.

    Product
    STEERING:CRITICAL FASTENERS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V186000·2023-03-20

    Kentucky Trailer XL-12 Recalled for Winch Remote Water Ingress Risk

    Kentucky Trailer is recalling 2021-2022 XL-12 trailers because water in the winch remote can cause corrosion and unintentional operation, increasing injury risk.

    Product
    KENTUCKY TRAILER — KENTUCKY TRAILER XL-12
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V183000·2023-03-20

    Prevost Recalls H3-45 Buses for Hazard Light Software Defect

    Prevost is recalling 2022-2023 H3-45 buses because hazard lights may not flash simultaneously when the ignition is off, increasing crash risk.

    Product
    PREVOST — PREVOST H3-45 VIP, H3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V187000·2023-03-20

    INFINITI QX50 and QX55 vehicles recalled for defective front door lock

    Nissan North America is recalling certain 2022 INFINITI QX50 and 2023 QX55 vehicles due to an incorrect door latch that may prevent the front right-side door from locking automatically, potentially allowing the door to open during a crash.

    Product
    INFINITI — INFINITI QX50, QX55
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V182000·2023-03-20

    Forest River Continental Cargo recalled for winch remote water intrusion

    Forest River Continental Cargo trailers with Warn wireless winch remotes are recalled. Water intrusion can corrode the remote's circuit board, causing unintended winch operation and injury risk.

    Product
    FOREST RIVER — FOREST RIVER CONTINENTAL CARGO, CARGO MATE, CROSS BOW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V184000·2023-03-20

    Prevost Recalls One 2023 H3-45 Bus for Emergency Exit Defect

    Prevost is recalling one 2023 H3-45 bus because the emergency exit window may require excessive force to open, potentially delaying escape during an emergency.

    Product
    PREVOST — PREVOST H3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V178000·2023-03-17

    Mercedes-Benz Recalls GLE and GLS Models for Rear Window Trim Defect

    Mercedes-Benz is recalling 70,225 GLE and GLS vehicles because rear door window trim bars may detach while driving, creating a road hazard.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH AMG GLS63 4MATIC+, GLS 580 4MATIC, GLS 450 4MATIC, AMG GLE63 S 4MATIC+
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V177000·2023-03-17

    Mercedes-Benz Recalls GLE and GLS Models for Fire Risk

    Mercedes-Benz is recalling certain 2020-2021 GLE and GLS models because incorrectly installed air conditioner drain hoses may cause water intrusion, increasing the risk of fire or electrical failure.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GLE63, GLE 580, MAYBACH GLS600, AMG GLE53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V180000·2023-03-17

    Hyundai Palisade windshield wiper motor failure due to ice and snow

    Hyundai is recalling 2021-2023 Palisade vehicles because the windshield wiper motor may fail due to snow or ice buildup, reducing visibility and increasing crash risk.

    Product
    HYUNDAI — HYUNDAI PALISADE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V175000·2023-03-17

    2020-2023 CAN-AM Spyder and Ryker Motorcycles Brake Light Defect

    CAN-AM is recalling 2020-2023 Spyder RT and 2022-2023 Ryker motorcycles because brake lights may remain illuminated when the brake pedal is not pressed. This can prevent other motorists from seeing actual braking and increase crash risk.

    Product
    CAN-AM — CAN-AM SPYDER RT, RYKER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23161·2023-03-17

    Mockingbird Single Strollers Recalled Due to Fall Hazard

    Mockingbird LLC is recalling about 25,390 Single Strollers because the lower side of the frame can crack, posing a fall risk to children. The company is offering a free frame reinforcement kit.

    Product
    Mockingbird Single Strollers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V179000·2023-03-17

    2023 Kia Carnival Recall: Tow Hitch Fire Risk

    Kia is recalling 2022-2023 Carnival vehicles with tow hitch harnesses that may accumulate water, causing electrical shorts that can result in fire.

    Product
    KIA — KIA CARNIVAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V176000·2023-03-17

    Porsche Taycan Seat Belt Warning System Malfunction Recall

    Porsche is recalling 2020-2023 Taycan models due to a malfunctioning seat belt warning system that may fail to alert unbelted passengers. Dealers will update the instrument cluster software free of charge.

    Product
    PORSCHE — PORSCHE TAYCAN 4S, TAYCAN GTS, TAYCAN TURBO, TAYCAN 4 CROSS TURISMO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V181000·2023-03-17

    Hyundai Santa Cruz and Santa Fe recalled for tow hitch fire hazard

    Hyundai is recalling 2019-2023 Santa Fe and related variants plus 2022-2023 Santa Cruz vehicles equipped with tow hitch harnesses. Water accumulation in the harness module may cause electrical short and fire.

    Product
    HYUNDAI — HYUNDAI SANTA FE PLUG-IN HYBRID, SANTA FE HYBRID, SANTA CRUZ, SANTA FE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V172000·2023-03-16

    2023 Cadillac XT6 Transmission Defect Recall for Half-Shaft Disengagement

    General Motors is recalling 2023 Cadillac XT6 and related vehicles due to a transmission defect. An incorrectly built sun gear can cause the half-shaft to disengage, risking loss of drive power or vehicle rollaway.

    Product
    CHEVROLET — CHEVROLET, CADILLAC, GMC BLAZER, XT5, XT6, TRAVERSE
    Category
    Vehicle
    Distribution
    Distributed nationwide