The Recall Desk

State

Northern Mariana Islands product recalls

73,106 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 73,106 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

12001–12025 of 73129

  • ModerateFDA (Devices)·Z-1335-2024·2024-03-27

    Angiodynamics Guidewire Introducer Devices Recalled for Manufacturing Defects

    Angiodynamics recalls MINI STICK MAX guidewire introducer devices due to manufacturing defects in the internal lumen that may prevent guidewire passage and delay surgical procedures.

    Product
    MINI STICK MAX 4F X 10 CM STD .018 NI/TU ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-750
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1346-2024·2024-03-27

    Guidewire Introducer Sheath from Angiodynamics Recalled for Manufacturing Defect

    Angiodynamics is recalling 65 units of its MINI STICK MAX guidewire introducer sheath due to manufacturing defects that may prevent guidewires from passing through during surgical procedures.

    Product
    MINI STICK MAX 5F X 10 CM STD .018 NI/TU ECHO 1.6" PG- Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-775
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1313-2024·2024-03-27

    Steris Endo Cleaning Indicator Recalled Due to Temperature Excursion

    Mckesson Medical-Surgical is recalling Steris Endo Cleaning Indicator VERIFY RESITEST devices due to temperature excursions that occurred on January 8, 2024. The temperature drop could cause the indicator to produce incorrect or delayed test results.

    Product
    Steris Corporation Endo Cleaning Indicator VERIFY" RESITEST"
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1311-2024·2024-03-27

    Sekisui OSOM BVBLUE Bacterial Vaginosis Control Kit recalled due to temperature exposure

    A Sekisui Diagnostics control kit for bacterial vaginosis testing was recalled after exposure to temperatures below the validated storage range for up to 60 minutes due to refrigerator mechanical failure.

    Product
    Sekisui Diagnostics Control Kit OSOM¿ BVBLUE¿ Bacterial Vaginosis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1315-2024·2024-03-27

    Laboratory Control Material Recalled Due to Temperature Storage Excursion

    Abbott Point of Care Control i-STAT Level 3 control material (Lot 121164) is being recalled due to temperature excursions in storage that could affect test accuracy. Affected units were distributed in Arizona, Pennsylvania, and Texas.

    Product
    Abbott Point of Care Control Control i-STAT¿ Level 3 1.7 mL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1339-2024·2024-03-27

    Angiodynamics surgical guidewire recalled for manufacturing defect

    Angiodynamics is recalling 5,176 units of MINI STICK MAX guidewires due to manufacturing voids that prevent passage through the introducer during surgery. Surgeons may need to exchange the sheath to complete procedures.

    Product
    MINI STICK MAX 5F X 10 CM STD .018 NI/TU ECHO 2.75" PG Catalog Number: 45-756
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1305-2024·2024-03-27

    Conductive Adhesive Gel Recalled Due to Thickness and Discoloration Issues

    Natus Neurology is recalling TENSIVE Conductive Adhesive Gel (Lot A0623009) after complaints of improper thickness, discoloration, and in one case, patient skin irritation following use.

    Product
    TENSIVE Conductive Adhesive Gel, REF 016-401600
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1306-2024·2024-03-27

    Natus Sleep Supplies Recalled for Conductive Adhesive Gel Quality Defects

    Natus Neurology is recalling Sleep Supplies Start Kits due to defective conductive adhesive gel supplied by Parker Laboratories. The gel is too thick, discolored, and caused patient irritation in at least one case.

    Product
    natus neurology, Sleep Supplies Start Kit with Single Use Supplies for Embla EX Series Amplifiers, REF 024252
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1344-2024·2024-03-27

    Guidewire Introducer Sheath with Manufacturing Defect Recalled by Angiodynamics

    Angiodynamics is recalling MINI STICK MAX guidewire introducer sheaths due to manufacturing defects that may prevent guidewire passage. The defect may cause procedural delays requiring equipment exchange during vascular interventions.

    Product
    MINI STICK MAX 5F X 10 CM STD .018 SS/SS NON-ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-767
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V230000·2024-03-25

    Doosan Portable Generator Trailers Recalled for Brake Wiring Defect

    Doosan is recalling 2015-2023 Portable Generator Trailers because the electric brake harness was incorrectly wired, potentially disabling brakes.

    Product
    DOOSAN PORTABLE POWER — DOOSAN PORTABLE POWER MOBILE GENERATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V225000·2024-03-24

    Mercedes-Benz Recalls 2023 Sprinter Vans for Electrical Fire Risk

    Daimler Vans USA is recalling 2023 Mercedes-Benz Sprinter vans because a 12-volt ground connection may overheat, increasing the risk of fire or loss of drive power.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 1500, SPRINTER 3500, SPRINTER 2500, SPRINTER 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V226000·2024-03-22

    Ford Recalls 2023-2024 Transit Vehicles for Tire Contact Defect

    Ford is recalling 2023-2024 Transit vehicles with the Trail package because tires may contact the wheel arch liner, risking tire damage and loss of control.

    Product
    FORD — FORD TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V223000·2024-03-22

    Ford Maverick and Bronco Sport tires may have been manufactured incorrectly

    Ford is recalling certain 2023 Maverick and Bronco Sport vehicles because the tires may have been manufactured incorrectly, which may result in a loss of vehicle handling and control.

    Product
    FORD — FORD MAVERICK, BRONCO SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V229000·2024-03-22

    Audi Recalls E-Tron GT Models Due to High-Voltage Battery Fire Risk

    Volkswagen Group of America is recalling 2022-2023 Audi E-Tron GT and RS E-Tron GT vehicles because a high-voltage battery short circuit could cause a fire.

    Product
    AUDI — AUDI RS E-TRON GT, E-TRON GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V228000·2024-03-22

    Audi e-tron GT high voltage battery modules may short circuit

    Volkswagen is recalling certain 2022-2024 Audi RS e-tron GT and e-tron GT vehicles because the high-voltage battery may experience a short circuit within the battery modules.

    Product
    AUDI — AUDI E-TRON GT, RS E-TRON GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V222000·2024-03-22

    Reading Truck Equipment Recalls 2021-2024 Dump Trucks Due to Fire Risk

    Reading Truck Equipment is recalling 2021-2024 dump body trucks because inadequate clearance may allow the hood to contact the main electrical fuse terminal, increasing the risk of a fire.

    Product
    READING TRUCK EQUIPMENT — READING TRUCK EQUIPMENT DUMP BODIED TRUCKS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24E028000·2024-03-22

    Suburban Recalls Slide-In Ranges with Overheating LED Backlight Boards

    Suburban is recalling certain Slide-In Range models because the LED backlight circuit board may overheat, increasing the risk of a fire.

    Product
    EQUIPMENT:APPLIANCE:OVEN/STOVE/COOKTOP recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V224000·2024-03-22

    Mercedes-Benz Recalls 2024 E-Class Vehicles for Wiring Harness Defect

    Mercedes-Benz is recalling 2024 E350 and E450 vehicles because the transmission wiring harness may be routed too close to the driveshaft, potentially causing a loss of drive power.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E 350, E 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V227000·2024-03-22

    Subaru Outback and Legacy occupant sensors may prevent airbag deployment

    Subaru is recalling certain 2020-2022 Outback and Legacy vehicles because an Occupant Detection System capacitor may crack and short circuit, preventing front passenger airbag deployment.

    Product
    SUBARU — SUBARU LEGACY, OUTBACK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V220000·2024-03-22

    Ford Mustang low pressure fuel supply lines may be damaged or cut

    Ford is recalling certain 2024 Mustang vehicles with 2.3L engines because the low-pressure fuel supply line may be damaged or cut, which can result in a fuel leak.

    Product
    FORD — FORD MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·24169·2024-03-21

    Happiness USA Roller Ball Candy Recalled Due to Choking Hazard

    Twenty Four Six Foods LLC is recalling all flavors of Happiness USA Liquid Rolling Candy because the rolling ball applicator can dislodge into a child's mouth, posing a choking hazard and risk of death.

    Product
    Happiness USA Liquid Rolling Candy
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·24171·2024-03-21

    Starbucks-branded metallic mugs recalled due to burn and laceration hazards

    Nestlé USA recalls about 440,500 metallic mugs from 2023 holiday Starbucks gift sets sold at Target, Walmart, and military retailers. The mugs can overheat or break when microwaved or filled with extremely hot liquid, causing severe burns and cuts. 10 people have been injured in 12 reported incidents.

    Product
    Metallic Mugs included in 2023 Holiday Starbucks-branded Gift Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-03212024-01·2024-03-21

    USDA Issues Public Health Alert for Ineligible Frozen Pangasius Maws

    USDA FSIS issued a public health alert for frozen striped pangasius maws illegally imported from China. The products are ineligible for entry and unfit for human consumption.

    Product
    FSIS Issues Public Health Alert for Ineligible Frozen Siluriformes Products Imported from the People’s Republic of China
    Category
    Food
    Distribution
    Distributed nationwide