The Recall Desk

State

North Dakota product recalls

20,364 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.

14751–14775 of 20364

  • ModerateFDA (Devices)·Z-0804-2023·2023-01-11

    C. difficile diagnostic kit recalled due to storage temperature deviation

    Biomerieux is recalling a C. difficile diagnostic test kit after units were stored outside temperature and time limits, potentially compromising test performance.

    Product
    PPM CLINICAL CRAPONNE CHROMID C.DIFFICILE 20 PLT, CATALOG 43871
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0809-2023·2023-01-11

    API NIT1 NIT2 Reagents Recalled Due to Improper Storage Conditions

    Biomerieux is recalling API NIT1 NIT2 Reagents (Catalog 70442, Batch 1009326520) distributed nationwide due to storage conditions that exceeded temperature and time parameters, preventing guaranteed product performance.

    Product
    API NIT1 NIT2 REAGENTS, CATALOG 70442
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0832-2023·2023-01-11

    Biomerieux Recalls BIOBALL K.RHIZOPHILA Diagnostic Kits Due to Storage Failure

    Biomerieux Inc recalls BIOBALL K.RHIZOPHILA diagnostic kits (batch 7408) due to exceeded temperature and time storage conditions that may compromise product performance.

    Product
    BIOBALL K.RHIZOPHILA (30X20), CATALOG 412690
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0826-2023·2023-01-11

    Levofloxacin ETEST Clinical Test Recalled for Improper Storage Conditions

    Biomerieux Inc. is recalling 7 units of ETEST CLINICAL LEVOFLOXACIN LE 32 US S30 diagnostic test kits (Batch 1009240000) due to temperature and time storage condition violations that prevent guarantee of product performance.

    Product
    ETEST CLINICAL LEVOFLOXACIN LE 32 US S30, CATALOG 412392
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0845-2023·2023-01-11

    Laboratory Testing Product Recall Due to Temperature Storage Excursion

    Biomerieux Inc is recalling PPM Lombard Products TSA 3P W Neutralizers due to storage temperature and time excursions that degrade product performance. Affected units cannot guarantee reliable testing results.

    Product
    PPM LOMBARD PRODUCTS TSA 3P W NEUTRALIZERS 100 PLT, CATALOG 419014
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0836-2023·2023-01-11

    FDA Recalls VITEK 2 AST-GN79 Reagent Test Kit for Temperature Excursion

    Biomerieux Inc. is recalling 310 units of the VITEK 2 REAGENT AST-GN79 TEST KIT (batches 5992201403 and 5992253503) nationwide because temperature and time conditions exceeded specified ranges, preventing guaranteed product performance.

    Product
    VITEK 2 REAGENT AST-GN79 TEST KIT 20 CARDS, CATALOG 413436
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0821-2023·2023-01-11

    ETEST Ceftriaxone Antibiotic Test Strips Recalled for Storage Condition

    Biomerieux is recalling ETEST Clinical Ceftriaxone test strips nationwide because storage temperature and time conditions were exceeded, which may affect product analytical performance.

    Product
    ETEST CLINICAL CEFTRIAXONE TX 32 US S30, CATALOG 412302
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0791-2023·2023-01-11

    VITEK 2 Reagent Test Kit Recalled Due to Storage Temperature and Time Exceedance

    Biomerieux Inc is recalling VITEK 2 Reagent NH Test Kit units nationwide because they were stored outside proper temperature and time parameters. Product performance cannot be guaranteed.

    Product
    VITEK 2 REAGENT NH TEST KIT VTK2 20 CARDS, CATALOG 21346
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0874-2023·2023-01-11

    PPM Lombard R2A Laboratory Medium Recalled for Exceeded Storage Conditions

    Biomerieux Inc is recalling PPM Lombard R2A medium products (lot 1009527290) because storage conditions exceeded acceptable parameters, compromising product performance. Approximately 20 units distributed nationwide in the United States.

    Product
    PPM LOMBARD PRODUCTS R2A MEDIUM 10PLT, CATALOG M1065
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0852-2023·2023-01-11

    Medical Device Recall: ETEST Meropenem/Vaborbactam Due to Storage Temperature Excursion

    Biomerieux is recalling 6 units of ETEST Meropenem/Vaborbactam susceptibility test kits (Batch 1008848690) distributed nationwide because they were stored outside specified temperature and time ranges, preventing guarantee of product performance.

    Product
    ETEST CLINICAL ETEST MEROPENEM/VABORBACTAM MEV US S30, CATALOG 421560
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0790-2023·2023-01-11

    VITEK 2 BCL Test Kit recalled for storage condition violations

    A batch of VITEK 2 Reagent BCL Test Kit from Biomerieux Inc is being recalled because storage conditions were exceeded, and product performance cannot be guaranteed.

    Product
    VITEK 2 REAGENT BCL TEST KIT VTK2 20 CARDS, CATALOG 21345
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0850-2023·2023-01-11

    Biomerieux Recalls VITEK 2 Diagnostic Test Kit Due to Storage Conditions

    Biomerieux Inc has recalled the VITEK 2 Reagent AST-GP78 Test Kit nationwide due to temperature and time storage exceedances that may affect product performance. No illnesses or injuries have been reported.

    Product
    VITEK 2 REAGENT AST-GP78 TEST KIT 20 CARDS, CATALOG 421051
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0802-2023·2023-01-11

    CHROMID MRSA Culture Medium Recalled for Storage Temperature Exceedance

    Biomerieux Inc is recalling PPM CLINICAL CHROMID MRSA 20 PLT diagnostic culture media (84 units) due to temperature and time exceedance during storage that may compromise product performance.

    Product
    PPM CLINICAL CHROMID MRSA 20 PLT US, CATALOG 43841
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V837000·2023-01-10

    2020-2023 IC Bus School Buses Recalled for Engine Shut Down Risk

    Navistar is recalling 2020-2023 IC Bus CESB school buses due to an engine control module defect that may cause unexpected engine shutdown while driving, increasing the risk of crashes and emergency evacuation situations.

    Product
    IC BUS — 2023 IC BUS CESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V766000·2023-01-10

    2022 RAM 1500 Front Seat Belt Retractors Recalled Due to Defect

    Certain 2022 RAM 1500 vehicles have front seat belt retractors with improperly welded components that may fail to restrain occupants during a crash. Chrysler is replacing the affected retractors free of charge.

    Product
    RAM — 2022 RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V772000·2023-01-10

    2022 Nissan Titan XD Infotainment Reboot Disables Rearview Display

    Nissan is recalling certain 2022 Titan XD and related models because the in-vehicle infotainment system may continuously reboot when restarted, causing the rearview display to become inoperative and reducing rear visibility.

    Product
    NISSAN — 2022 NISSAN TITAN XD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V835000·2023-01-10

    Tesla Model 3 and Model Y suspension fasteners recalled for loosening

    Tesla is recalling 2019-2021 Model 3 and 2020-2021 Model Y vehicles where front suspension lateral link fasteners may loosen, potentially causing wheel misalignment and increasing crash risk.

    Product
    TESLA — 2020 TESLA MODEL 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V768000·2023-01-10

    Jeep Wrangler Plug-In Hybrid Battery Fuse Defect Increases Crash Risk

    Chrysler is recalling the 2022-2023 Jeep Wrangler PHEV for battery fuse defects caused by incorrect fasteners. The fuses can overheat and fail, causing loss of drive power and increasing the risk of a crash.

    Product
    JEEP — 2023 JEEP WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V834000·2023-01-10

    2020-2023 Tesla Model 3 Curtain Airbag Deployment Safety Defect

    Tesla is recalling certain 2020-2023 Model 3 vehicles because the side curtain airbag may be improperly secured to the roof rail and could twist, deploying incorrectly during a crash and increasing risk of injury or ejection.

    Product
    TESLA — 2020 TESLA MODEL 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V767000·2023-01-10

    2022 Jeep Wrangler Fuel Pump Engine Stall Recall

    Chrysler is recalling 2020-2022 Jeep Wranglers, Gladiators, and Ram 1500s due to potential fuel pump failure that may cause engine stall, increasing crash risk. Dealers will replace the pump at no cost.

    Product
    JEEP — 2022 JEEP WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·23089·2023-01-09

    Kids2 Rocking Sleepers Recalled After 15 Infant Deaths

    Kids2 is recalling approximately 694,000 Rocking Sleepers after 15 infant fatalities were reported. Infants died after rolling from their back to their stomach or side while unrestrained.

    Product
    All models of Kids2 Rocking Sleepers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·23088·2023-01-09

    Fisher-Price Recalls 4.7 Million Rock 'n Play Sleepers Due to Infant Deaths

    Fisher-Price is recalling approximately 4.7 million Rock 'n Play Sleepers after at least 8 deaths were reported following the initial April 2019 recall announcement. Infants have died after rolling from their back to their stomach or side while unrestrained.

    Product
    All models of Rock 'n Play Sleepers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V615000·2023-01-09

    2023 Porsche Taycan battery sealant defect increases fire risk

    Porsche is recalling 2023 Taycan vehicles with high-voltage batteries that may have insufficient sealant, allowing liquid accumulation that can cause electrical arcing and fire risk. Dealers will test and replace batteries free of charge.

    Product
    PORSCHE — 2023 PORSCHE TAYCAN 4S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V612000·2023-01-09

    2022 Silver Lake Travel Trailers Recalled for Detaching Sidewall Siding

    Forest River's 2022 Silver Lake and Della Terra travel trailers are being recalled because the aluminum sidewall siding may not be properly installed and could detach. Detached siding increases the risk of a crash or injury while towing.

    Product
    EAST TO WEST — 2022 EAST TO WEST SILVER LAKE
    Category
    Vehicle
    Distribution
    Distributed nationwide