The Recall Desk

State

Northern Mariana Islands product recalls

73,219 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 73,219 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

16126–16150 of 73242

  • HighNHTSA·23V343000·2023-05-12

    Fox Factory Recalls Winch Remotes on 2021-2023 Jeep, GM, Ford, RAM Vehicles

    Fox Factory is recalling 1,578 vehicles equipped with Warn winches because water may enter the remote, corrode the circuit board, and cause the winch to operate unintentionally.

    Product
    FOX FACTORY — FOX FACTORY FORD PICKUP, GM PICKUP, RAM PICKUP, JEEP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V342000·2023-05-12

    2020-2023 Ford Explorer and Lincoln Vehicles Rearview Camera Failure

    The rearview camera video output may fail on certain 2020-2023 Ford Explorer and Lincoln vehicles, reducing rear visibility and increasing crash risk. Ford will replace the camera free of charge.

    Product
    LINCOLN — LINCOLN, FORD AVIATOR, EXPLORER, CORSAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23201·2023-05-11

    Peloton Exercise Bikes Recalled for Seat Post Breakage and Fall Risk

    Peloton is recalling approximately 2.2 million Model PL01 exercise bikes because the seat post assembly can break during use, causing users to fall. The company has received 35 reports of seat post breakage, including 13 reports of injuries such as fractured wrists, lacerations, and bruises.

    Product
    Peloton Bikes Model PL01
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V338000·2023-05-11

    Jeep Cherokee Recall: Power Liftgate Electrical Short Fire Risk

    Chrysler is recalling 2014-2016 Jeep Cherokee vehicles with power liftgates due to an electrical short that may cause a fire. Owners should park outside until repairs are completed.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23755·2023-05-11

    Ski-Doo Snowmobiles Recalled for Fire Hazard from Fuel Leaks

    BRP U.S. Inc. is recalling about 12,500 Ski-Doo snowmobiles from model years 2021 and 2022 because a fuel injector hose retainer screw can loosen, cause fuel leaks, and pose a fire hazard. Four fires have been reported.

    Product
    Ski-Doo snowmobiles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V337000·2023-05-11

    BMW Recalls 2007-2014 MINI Cooper Models for Fire Risk

    BMW is recalling 2007-2014 MINI Cooper models because a short-circuit in the driver's footwell may cause a fire. Owners should contact dealers for inspection and repair.

    Product
    MINI — MINI COOPER CLUBMAN, COOPER, COOPER S, JCW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·017-2023·2023-05-11

    Eastern Meat Solutions Recalls Raw Boneless Pork Products Imported Without Reinspection

    Eastern Meat Solutions is recalling approximately 40,763 pounds of raw, boneless pork products imported from Canada without FSIS import reinspection. No adverse reactions have been reported.

    Product
    Eastern Meat Solutions, Inc. Recalls Raw, Boneless Pork Products Imported Without Benefit of Import Reinspection
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·23V340000·2023-05-11

    Altec Recalls 2021-2023 Digger Derricks Due to Boom Pressure Limiter Defect

    Altec is recalling 2021-2023 Digger Derricks because a defective boom pressure limiter may allow lifting loads above rated capacity, increasing the risk of unit instability and injury.

    Product
    ALTEC — ALTEC DIGGER DERRICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23756·2023-05-11

    Advanced EV Advent Golf Carts Recalled for Loose Front Seat Hazard

    Advanced EV is recalling approximately 2,500 Advent 4 and 6-passenger golf carts sold from May 2020 through June 2022 because the front seat can become loose due to missing rubber grommets, posing fall and injury risks.

    Product
    Advent 4F, Advent 4FL, Advent 6 and Advent 6L golf carts
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V336000·2023-05-11

    Jeep Grand Cherokee 2023 Model Recalled for Missing Air Bag Warning Label

    Certain 2023 Jeep Grand Cherokee and 2022 Grand Cherokee 4XE vehicles may be missing the required air bag warning label. The missing label could prevent occupants from understanding proper restraint usage, potentially increasing injury risk in a crash.

    Product
    JEEP — JEEP GRAND CHEROKEE, GRAND CHEROKEE 4XE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V339000·2023-05-11

    Child seat anchor defect affects 2020-2023 Chevrolet Equinox and GMC Terrain

    General Motors is recalling 2020-2023 Chevrolet Equinox and GMC Terrain vehicles due to excessive powder coating on rear child seat LATCH anchorage bars, which could prevent proper installation and leave child seats unsecured in a crash.

    Product
    CHEVROLET — CHEVROLET, GMC EQUINOX, TERRAIN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23200·2023-05-11

    Positec Recalls Blue Ridge Utility Knives Due to Laceration Hazard

    Positec USA Inc. is recalling about 36,250 Blue Ridge utility knives sold at Target because the blade can become unlocked and protrude through the original packaging, causing laceration injuries. Two reports of blade protrusion and resulting lacerations have been received.

    Product
    Blue Ridge utility knives
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23198·2023-05-11

    World Market Cocktail Shakers Recalled Due to Laceration Hazard

    World Market is recalling about 6,300 Gold Metal and Ribbed Glass Cocktail Shakers because the glass can crack and break during use, posing a laceration hazard. The firm has received three reports of cracking or breaking, including two incidents of lacerations that did not require medical attention.

    Product
    Gold Metal and Ribbed Glass Cocktail Shakers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23199·2023-05-11

    American Woodmark Kitchen Wall Cabinets Recalled for Detachment Risk

    American Woodmark Corporation is recalling about 235,000 Continental Cabinets and Hampton Bay kitchen wall cabinets that can detach from walls, posing an impact hazard. The company will provide free repair kits with brackets and installation assistance.

    Product
    Continental Cabinets and Hampton Bay Kitchen Wall Cabinets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0572-2023·2023-05-10

    NUX Male Enhancement Capsules Recalled for Undeclared Prescription Ingredients

    The FDA recalls NUX Male Enhancement capsules distributed nationwide because they contain undeclared sildenafil and tadalafil, making them an unapproved drug. Consumers should not use this product.

    Product
    NUX Male Enhancement capsule, 1-count blister card, distributed by SX Power CO., Chicago, Il 60612, UPC 6 01577 51236 3.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0571-2023·2023-05-10

    Pro Power Knight Plus Capsule Recalled for Undeclared Pharmaceutical Ingredients

    Pro Power Knight Plus capsules contain undeclared sildenafil and tadalafil, prescription ingredients not listed on the label. The product was marketed as an unapproved drug and poses safety risks.

    Product
    Pro Power Knight Plus capsule, 2550mg, 1-count blister card, Distributed by Beyond Health and youth Inc, Seattle, WA 98110, UPC 4 94922 90522 0.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V334000·2023-05-10

    GM Recalls 2014-2017 SUVs for Driver Air Bag Inflator Defect

    General Motors is recalling 2014-2017 Buick Enclave, Chevrolet Traverse, and GMC Acadia vehicles because the driver's air bag inflator may explode during deployment.

    Product
    BUICK — BUICK, CHEVROLET, GMC ENCLAVE, TRAVERSE, ACADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0573-2023·2023-05-10

    Unapproved Drug Capsule Recalled for Undeclared Sexual Enhancement Ingredients

    DYNAMITE SUPER capsule is being recalled nationwide because it was marketed without FDA approval and contains undeclared sildenafil and tadalafil, active ingredients used in sexual enhancement products.

    Product
    DYNAMITE SUPER capsule, 58,000 MG, 1-count blister card, Made in America, UPC 6 75799 37602 7.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·016-2023·2023-05-10

    Mitten Gourmet Recalls Ready-to-Eat Pork Rinds Produced Without Federal Inspection

    Mitten Gourmet is recalling approximately 1,137 pounds of ready-to-eat pork rinds because they were produced without the benefit of federal inspection. Consumers are urged to discard or return the products.

    Product
    Mitten Gourmet, LLC, Recalls Ready-to-Eat Pork Rind Products Produced without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1476-2023·2023-05-10

    Steris Light Handle Covers May Detach During Surgical Use

    Steris Corporation is recalling 263,280 surgical light handle covers worldwide because they may separate from the light handle during procedures, potentially compromising the sterile field.

    Product
    Steris Lighting and Visualization Systems, Sterile Light handle Cover LB44 -Sterilizable consumables (disposable, single use) used to drape the lighthandle of STERIS surgical lighting systems for the purpose of maintaining a sterile surgical environment. REF: LB44
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1505-2023·2023-05-10

    Siemens ADVIA Centaur Cortisol Diagnostic Kits Recalled for Negative Measurement Bias

    Siemens Healthcare Diagnostics is recalling 18,961 ADVIA Centaur Cortisol diagnostic kits due to negative bias in urine samples causing intermittently low test results that could affect clinical diagnosis.

    Product
    ADVIA Centaur Cortisol 50T (Material Number 10994924), ADVIA Centaur Cortisol 250T (Material Number 10994926), and ADVIA Centaur Cortisol REF 250T (Material Number 10994927). In vitro diagnostic use in the quantitative determination of cortisol in human serum, plasma (EDTA and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1498-2023·2023-05-10

    Angiography System C-Arm Positioning Malfunction May Cause Patient Injury

    Siemens ARTIS pheno angiography systems may misposition the C-arm by 5-10 millimeters when using the reference image positioning function, risking patient and staff crushing injuries. The device may also display inaccurate imaging overlays, potentially causing vessel perforation.

    Product
    ARTIS pheno systems with a Siemens Healthineers table or Trumpf/MAQUET table (OEM)- Angiography systems developed for single and biplane diagnostic imaging and interventional procedures. Model: 10849000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1503-2023·2023-05-10

    FDA Class II Recall: Ultraview SL Command Module Monitoring Alarms May Fail

    Spacelabs Healthcare is recalling 1,088 Ultraview SL Command Module units due to a software defect. The devices may fail to display alarms or waveforms when parameter processing is suspended, potentially causing clinicians to miss critical patient events.

    Product
    Ultraview SL (UVSL) Command Module, Model 91496
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0788-2023·2023-05-10

    Soy Flour Recalled for Undeclared Gluten in Gluten-Free Products

    Cargill is recalling PROSANTE TSOYFLR flour products labeled gluten-free because they may contain gluten above 20 ppm. Consumers with celiac disease or gluten sensitivity should not consume these products.

    Product
    PROSANTE TSOYFLR 3P MNCD 50LB BG, paper bag
    Category
    Food
    Distribution
    Distributed nationwide