The Recall Desk

State

Northern Mariana Islands product recalls

73,198 recalls have nationwide distribution and so reach Northern Mariana Islands. 23 additional recalls listed Northern Mariana Islands specifically in their distribution scope.

What the numbers show

Total
23
Critical
0
Severe
8
Most recent
2026-09-23

Of the 23 recalls naming Northern Mariana Islands we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 8 (35%) are Severe.

Which agencies issued them

These figures cover only the 23 recalls whose distribution notice names Northern Mariana Islands specifically. The 73,198 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

14301–14325 of 73221

  • SevereNHTSA·23V625000·2023-09-08

    2025 Ford E-350 Recalled for Transmission Park Pawl Defect

    Ford is recalling 2025 E-350 trucks and related models due to a transmission park pawl casting defect that may not fully engage, potentially causing vehicle rollaway.

    Product
    FORD — FORD E-350, F-750 SD, F-650 SD, F-650 INCOMPLETE CHASSIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V626000·2023-09-08

    Lincoln Aviator and Ford Explorer battery defect poses fire and power-loss risk

    Ford is recalling 2020-2022 Lincoln Aviators and Ford Explorers with 3.0L plug-in hybrid engines. A high-voltage battery manufacturing defect may cause battery failure, loss of drive power, and fire risk.

    Product
    FORD — FORD, LINCOLN EXPLORER, AVIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V628000·2023-09-08

    Nissan Altima and Sentra rearview camera harness defect increases crash risk

    Nissan is recalling certain 2019-2021 Altima and 2020-2021 Sentra vehicles because the rearview camera harness can become damaged, preventing the camera display from working. This reduces rear visibility and increases the risk of crashes when backing.

    Product
    NISSAN — NISSAN SENTRA, ALTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V623000·2023-09-07

    2023-2024 Alfa Romeo Tonale plug-in hybrid electric vehicles recalled for fire risk

    Chrysler is recalling 2023-2024 Alfa Romeo Tonale and Dodge Hornet plug-in hybrid electric vehicles. Improperly tightened battery and high voltage connector cables can overheat and cause fires while parked or driving.

    Product
    DODGE — DODGE, ALFA ROMEO HORNET, TONALE PHEV, TONALE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V624000·2023-09-07

    Midwest Fire Recalls 2022-2023 All-Poly Series Tanker-Pumper Fire Trucks

    Midwest Fire is recalling 2022-2023 All-Poly Series Tanker-Pumper fire trucks due to a software error that may cause a sudden loss of drive power, increasing the risk of a crash.

    Product
    MIDWEST FIRE — MIDWEST FIRE ALL-POLY SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·042-2023·2023-09-07

    USDA Recalls Frozen Pork Products Imported Without Reinspection

    Empacadora Frape, USA LLC is recalling approximately 20,455 pounds of frozen pork chicharron and carnitas that were imported without the required reinspection.

    Product
    Empacadora Frape, USA LLC, Recalls Pork Products Imported Without Benefit of Import Reinspection
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·23790·2023-09-07

    ARGO Xplorer ATVs Recalled for Fire Hazard from Fuel Overflow

    ARGO USA Inc. is recalling about 500 ARGO Xplorer ATVs due to incorrectly installed check valves and vent hoses that can cause fuel overflow and pose a fire hazard. The firm has received two reports of fuel overflow incidents, including one fire, with no injuries reported.

    Product
    ARGO Xplorer ATVs
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23791·2023-09-07

    Whirlpool ADC Commercial Clothes Dryers Recalled for Fire Hazard

    Whirlpool has recalled about 2,500 ADC brand 30 lb. capacity stacked commercial clothes dryers because they can overheat and ignite clothes, creating a fire hazard. The company has received two reports of fuel overflow incidents, including one fire, with no injuries reported.

    Product
    ADC brand 30 lb. capacity stacked commercial clothes dryers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23276·2023-09-07

    Pirelli P ZERO Race TLR Bicycle Tires Recalled for Fall Hazard

    Pirelli is recalling about 14,500 P ZERO Race TLR bicycle tires because the tire bead can unseat from the rim, causing rapid air loss and loss of control. Consumers should stop using the tires and contact Pirelli for a free replacement or refund.

    Product
    Pirelli P ZERO Race TLR Bicycle Tires
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V622000·2023-09-07

    2023-2024 BMW Models Recall: Front Passenger Knee Air Bag Deployment Failure

    BMW is recalling certain 2023 BMW XM and 2024 BMW X5, X6, X7, and Alpina XB7 vehicles because the front passenger knee air bag may not deploy as intended, increasing injury risk in a crash.

    Product
    BMW — BMW X6, XM, X5, X7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23789·2023-09-07

    Lectric eBikes Disc Brake Calipers Recalled for Crash and Injury Hazards

    Lectric eBikes is recalling about 45,000 disc brake calipers on certain e-bicycle models because the brakes can fail, causing loss of control and crashes. The firm has received four reports of lost braking power, including two injuries.

    Product
    Disc brake calipers sold on Lectric e-bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23274·2023-09-07

    Emporia Smart Plugs Recalled Due to Electric Shock Hazard

    Emporia Energy Corp. is recalling about 80,000 smart plugs sold online from July 2022 through May 2023 because they are not adequately grounded and can pose an electric shock hazard.

    Product
    Emporia Smart Plugs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V620000·2023-09-06

    Ducati Recalls 2018-2020 XDiavel Motorcycles for Side Stand Bracket Failure

    Ducati is recalling 2018-2020 XDiavel and XDiavel S motorcycles because a side stand bracket may fail, causing the stand to open while riding and shutting down the engine.

    Product
    DUCATI — DUCATI XDIAVEL S, XDIAVEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2435-2023·2023-09-06

    Intra-Aortic Balloon Pumps recalled for unexpected gas loss and gain alarms

    Datascope's Cardiosave Hybrid Intra-Aortic Balloon Pumps may trigger unexpected alarms indicating gas loss or gain due to undocumented causes including patient movement and blood in the circuit. The FDA Class I recall affects 9,175 units.

    Product
    Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-31, 0998-UC-0800-31, 0998-00-0800-32, 0998-00-0800-33, 0998-UC-0800-33, 0998-00-0800-34, 0998-00-0800-35, 0998-00-0800-45, 0998-00-0800-52, 0998-UC-0800-52, 0998-00-0800-53, 0998-UC-0800-53…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2432-2023·2023-09-06

    Cardiosave Rescue Intra-Aortic Balloon Pumps Fail to Charge When Improperly Inserted

    Datascope Corp. is recalling 9,175 units of Cardiosave Rescue IABP devices because batteries will not charge if the console is not fully inserted into the hospital cart. Users were often unaware of this insertion requirement.

    Product
    Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2436-2023·2023-09-06

    Cardiosave Rescue IABP Alarms May Trigger Unexpectedly During Therapy

    Datascope Corp. is recalling approximately 9,175 Cardiosave Rescue IABPs because unexpected gas-loss and gas-gain alarms may occur during therapy due to patient movement, blood in the circuit, and hardware issues.

    Product
    Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2467-2023·2023-09-06

    EVIS EXERA III Duodenovideoscope Recalled Due to Patient Infection Reports

    Olympus Corporation recalls 6,426 units of the EVIS EXERA III Duodenovideoscope (Model TJF-Q190V) due to recent reports of patient infections. The device was distributed nationwide in the United States.

    Product
    EVIS EXERA III DUODENOVIDEOSCOPE OLYMPUS TJF-Q190V
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1150-2023·2023-09-06

    Vegetal Vigra Capsules Recalled for Containing Unapproved Sildenafil

    The FDA is recalling Vegetal Vigra 200mg capsules nationwide because they contain sildenafil, an active ingredient in FDA-approved medications. The product was marketed without FDA approval.

    Product
    Vegetal Vigra, 200mg capsules, 8-count bottle, Manufacturer: Hand-shaking (Int'l) Corp. USA ADD: Hand-shaking Mansion, the 5th Ave., Stanford, USA. UPC 8 931028 556885
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2431-2023·2023-09-06

    Cardiosave Hybrid Intra-Aortic Balloon Pump charging issue recall

    The Cardiosave Hybrid Intra-Aortic Balloon Pump console fails to charge if not fully inserted into the hospital cart. Users unaware of this requirement may attempt to use a non-charged device during critical cardiac care.

    Product
    Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-31, 0998-UC-0800-31, 0998-00-0800-32, 0998-00-0800-33, 0998-UC-0800-33, 0998-00-0800-34, 0998-00-0800-35, 0998-00-0800-45, 0998-00-0800-52, 0998-UC-0800-52, 0998-00-0800-53, 0998-UC-0800-53…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2438-2023·2023-09-06

    Cardiosave Rescue Intra-Aortic Balloon Pumps Recalled Due to Autofill Failure

    Datascope Corp. is recalling 9,175 Cardiosave Rescue Intra-Aortic Balloon Pumps due to autofill failures that can cause the pump to stop.

    Product
    Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2437-2023·2023-09-06

    Cardiosave Hybrid Intra-Aortic Balloon Pumps recalled for autofill failure

    Datascope Corp. is recalling Cardiosave Hybrid intra-aortic balloon pumps due to autofill failure causing pump stops. The FDA Class I recall affects approximately 9,175 units distributed nationwide.

    Product
    Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-31, 0998-UC-0800-31, 0998-00-0800-32, 0998-00-0800-33, 0998-UC-0800-33, 0998-00-0800-34, 0998-00-0800-35, 0998-00-0800-45, 0998-00-0800-52, 0998-UC-0800-52, 0998-00-0800-53, 0998-UC-0800-53…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2433-2023·2023-09-06

    Cardiosave Hybrid IABP devices recalled for temperature and pumping function failures

    Datascope is recalling Cardiosave Hybrid intra-aortic balloon pumps due to reported temperature alarms that can cause loss of pumping function or unexpected standby mode. Users have reported these system failures in critical cardiac support devices.

    Product
    Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-31, 0998-UC-0800-31, 0998-00-0800-32, 0998-00-0800-33, 0998-UC-0800-33, 0998-00-0800-34, 0998-00-0800-35, 0998-00-0800-45, 0998-00-0800-52, 0998-UC-0800-52, 0998-00-0800-53, 0998-UC-0800-53…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2434-2023·2023-09-06

    Cardiosave Rescue IABP Pumps Recalled for System Overheating and Pump Failure

    Datascope Corp. is recalling Cardiosave Rescue Intra-Aortic Balloon Pumps due to system overheating alarms that can cause loss of pumping function and device shutdown.

    Product
    Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85, 0998-UC-0800-75, 0998-UC-0800-83, 0998-UC-0800-85,
    Category
    Medical Device
    Distribution
    Distributed nationwide