The Recall Desk

State

Northern Mariana Islands product recalls

73,824 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
18
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 18 (78%) are Severe.

Which agencies issued them

These figures cover only the 23 recalls whose distribution notice names Northern Mariana Islands specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

52576–52600 of 73847

  • SevereNHTSA·15V516000·2015-08-13

    Pierce Emergency Vehicles Recalled for Driveshaft Defect

    Pierce is recalling 2014-2015 emergency vehicles because a driveshaft may bend or twist, potentially causing loss of drive and road hazards.

    Product
    PIERCE — PIERCE DASH CF, ENFORCER, VELOCITY, ARROW XT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V512000·2015-08-13

    Terex Recalls 2013-2015 Digger Derrick and Aerial Devices Trucks

    Terex is recalling 386 model year 2013-2015 Digger Derrick and Aerial Devices trucks because vertical cylinders may drift when loaded, risking platform falls.

    Product
    TEREX — TEREX DIGGER DERRICK, AERIAL DEVICES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·15213·2015-08-13

    Ambient Weather Recalls Radios Due to Fire Hazard

    Ambient Weather is recalling about 12,500 weather radios because the AC power adapter can overheat, posing a fire hazard. Consumers should stop using the radios and contact the company for a free replacement adapter.

    Product
    Ambient Weather radios
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V515000·2015-08-13

    Toyota Recalls 4Runners Due to Accessory Exhaust Tip Burn Risk

    Southeast Toyota Distributors is recalling 2010-2015 Toyota 4Runners because accessory exhaust tips may contact people and cause burns.

    Product
    TOYOTA — TOYOTA 4RUNNER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V513000·2015-08-13

    AEV Trauma Hawk Recalled for Reversed Backup Camera Images

    Halcore Group is recalling 2014-2015 AEV Trauma Hawk emergency vehicles because the backup camera may display reversed images, increasing crash risk.

    Product
    AEV — AEV TRAUMAHAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2319-2015·2015-08-12

    Cook Inc. Recalls Slip-Cath Beacon Tip Catheters Due to Tip Separation

    Cook Inc. is recalling Slip-Cath Beacon Tip Catheters because the tips may split or separate, potentially causing loss of function or complications.

    Product
    Slip-Cath Beacon Tip Catheter. Angiographic catheter. For use in angiographic procedures as a conduit for the delivery of contrast media and can help physicians diagnose occlusion or stenosis. The catheters are designed for percutaneous introduction into the vascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2943-2015·2015-08-12

    Anabolic Science Labs Recalls Slim X Lean Hour Energy Drink

    Anabolic Science Labs is recalling Slim X Lean Hour 12+ Hour Energy products due to undeclared synthetic hormone ingredients.

    Product
    "***SLIM X LEAN HOUR 12+ HOUR ENERGY***PRODUCT ID: ASL-SXL-03***Manufactured for: ASL ANABOLIC SCIENCE LABS WINTER PARK, FL 32789***
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2318-2015·2015-08-12

    Cook Inc. Recalls Beacon Tip Royal Flush Plus High-Flow Catheters

    Cook Inc. is recalling Beacon Tip Royal Flush Plus High-Flow Catheters due to reports of tip splits or separation that may cause loss of function or complications.

    Product
    Beacon Tip Royal Flush Plus High-Flow Catheter. Angiographic catheter. For use in angiographic procedures as a conduit for the delivery of contrast media and can help physicians diagnose occlusion or stenosis. The catheters are designed for percutaneous introduction into…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2325-2015·2015-08-12

    Medtronic Passive Biopsy Needle Kit Recalled for Adhesive Defect

    Medtronic is recalling 1,415 Passive Biopsy Needle Kits because adhesive failure may cause the sphere assembly to move, leading to inaccurate navigation during brain biopsies.

    Product
    Medtronic Passive Biopsy Needle Kit, Part Number 9731754 - Passive Biopsy Fee Per Use (FPU) Kit. The image guided Passive Biopsy Needle is an accessory instrument with the StealthStation System. The Biopsy Needle is intended to be used for stereotaxy biopsy of brain tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2326-2015·2015-08-12

    Aesculap S4C Occiput Torque Wrench Recalled Due to Reassembly Defect

    Aesculap is recalling 10 S4C Occiput Torque Wrenches because improper reassembly after reprocessing caused a screw to break during implantation.

    Product
    S4C Occiput Torque Wrench F/Set Screw; used to tighten the S4 Cervical Spinal System clamping screws with a defined torque 2.8 Nm for tightening the clamping screw in the screw head/hook head/occipital plate/transverse connector and other connectors.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2317-2015·2015-08-12

    Cook Inc. Recalls Beacon Tip Torcon NB Advantage Catheters

    Cook Inc. is recalling Beacon Tip Torcon NB Advantage Catheters due to reports of tip splits or separation, which may cause loss of function or complications.

    Product
    Beacon Tip Torcon NB Advantage Catheter. Angiographic catheter. For use in angiographic procedures as a conduit for the delivery of contrast media and can help physicians diagnose occlusion or stenosis. The catheters are designed for percutaneous introduction into the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2324-2015·2015-08-12

    Medtronic Passive Biopsy Needle Kit Recalled for Adhesive Defect

    Medtronic is recalling 1,415 Passive Biopsy Needle Kits because compromised adhesive may cause the sphere assembly to move, leading to inaccurate navigation during brain biopsies.

    Product
    Medtronic Passive Biopsy Needle Kit, Part Number 9733068 - Passive Biopsy Needle Kit. The image guided Passive Biopsy Needle is an accessory instrument with the StealthStation System. The Biopsy Needle is intended to be used for stereotaxy biopsy of brain tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2264-2015·2015-08-12

    Medtronic Recalls EnVeo R Loading Systems Due to Particulate Presence

    Medtronic is recalling EnVeo R Loading Systems because of the presence of particulate. The recall affects 6,912 units worldwide, including 540 in the US.

    Product
    EnVeo R Loading System, Model No. LS-EnVeoR-23, LS-EnVeoR-2629, LS-EnVeoR-23-C, LS-EnVeoR-2629-C. Cardiovascular valve delivery system for use with the Medtronic CoreValve Evolut R system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V508000·2015-08-12

    Jeep Renegade Recall for Radio Software Vulnerability

    Chrysler is recalling 2015 Jeep Renegade vehicles to fix a radio software vulnerability that could allow unauthorized remote control of vehicle systems.

    Product
    JEEP — JEEP RENEGADE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2342-2015·2015-08-12

    Siemens Axiom Artis Angiography Systems Recalled for Liquid Seepage Risk

    Siemens Medical Solutions is recalling Axiom Artis angiography systems because liquid may seep through the top cover and penetrate internal components, potentially disabling table movements.

    Product
    Axiom Artis systems, dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures that can be performed include cardiac angiography, neuro angiography…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V511000·2015-08-12

    Pierce Velocity and Quantum Vehicles Recalled for Headlight Flickering

    Pierce is recalling 2014-2015 Velocity and Quantum vehicles because LED headlamps may flicker in extreme cold, reducing visibility and increasing crash risk.

    Product
    PIERCE — PIERCE VELOCITY, QUANTUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2344-2015·2015-08-12

    Siemens ACUSON S Family Ultrasound Systems Recalled for Biopsy Guide Defect

    Siemens is recalling ACUSON S Family ultrasound systems because biopsy needles may move outside the on-screen guidelines when using specific attachments.

    Product
    ACUSON S Family ultrasound systems utilizing the 18L6 HD and/or 6C1 HD biopsy guidelines 6C1HD - model numbers: 10442008 6C1HD Needle Guide, S3000; 10440586 6C1 HD Biopsy Guide, S2000 18L6 - model numbers: 10442007 18L6 Biopsy Guide, S3000 10044200 S2000 Biopsy Starter…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2340-2015·2015-08-12

    Siemens Artis zee Systems Recalled for Potential Liquid Seepage

    Siemens Medical Solutions is recalling Artis zee angiography systems because liquid may seep through the table cover, potentially preventing table movement.

    Product
    Siemens Artis zee systems; dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures that can be performed include cardiac angiography, neuro…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V507000·2015-08-12

    Nissan Recalls Versa and Versa Note for Pedal Interference Risk

    Nissan is recalling 2012-2015 Versa and 2014-2015 Versa Note vehicles because a center console trim panel may catch the driver's shoe, delaying brake application and increasing crash risk.

    Product
    NISSAN — NISSAN VERSA, VERSA NOTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1283-2015·2015-08-12

    Teva Recalls Amphetamine Tablets Due to Unknown Impurity

    Teva Pharmaceuticals is recalling specific lots of amphetamine tablets because they failed impurity specifications. The product contains an unknown impurity.

    Product
    DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE — DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE (DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2347-2015·2015-08-12

    Merge Hemo System Recalled for Freeze-Up During Cardiac Procedures

    Merge Healthcare is recalling 451 Merge Hemo systems used with Masimo PHASEIN modules due to system freeze-ups that required moving patients to other cath labs.

    Product
    Merge Hemo, 9.10, 9.20.0, 9.20.1,9.20.2, 9.30, 9.40.0, 9.40.1, 9.40.2 with Massimo PHASEIN End Tidal CO2 (EtCO2) module. Merge Hemo (formerly named HeartSuite Hemodynamics) monitors, measures, and records physiologic data from a human patient undergoing a cardiac…
    Category
    Medical Device
    Distribution
    Distributed nationwide