The Recall Desk

State

Northern Mariana Islands product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

54976–55000 of 73850

  • SevereNHTSA·15V165000·2015-03-23

    Navistar Recalls 2015-2016 International Trucks Due to Brake Fire Risk

    Navistar is recalling 2015-2016 International and IC Bus vehicles because defective brake actuators may cause dragging, overheating, and wheel end fires.

    Product
    INTERNATIONAL — INTERNATIONAL, IC BUS TRANSTAR, CE, DURASTAR, WORKSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V168000·2015-03-23

    Navistar Recalls 2015 IC RE Transit Buses for Brake Hose Defect

    Navistar is recalling 2015 IC RE non-school Transit Buses because the front air brake hose may contact the tire, causing leaks and increased crash risk.

    Product
    IC BUS — IC BUS RECB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V166000·2015-03-23

    Navistar Recalls 2015-2016 IC School Buses for Brake Fire Risk

    Navistar is recalling specific 2015-2016 IC school buses because defective air brake actuators may cause dragging brakes and wheel end fires.

    Product
    IC BUS — IC BUS CASB, CESB, RESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V164000·2015-03-23

    GM Recalls 2013-2015 Chevrolet Malibu for Sunroof Pinch Hazard

    General Motors is recalling 2013-2015 Chevrolet Malibus because the sunroof switch may be pressed inadvertently, causing the roof to close unexpectedly and risk pinch injuries.

    Product
    CHEVROLET — CHEVROLET MALIBU
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V159000·2015-03-20

    Charles Machine Recalls Ditch Witch T26 Trailers Due to Bearing Defect

    Charles Machine is recalling 2002-2015 Ditch Witch T26 trailers because incorrect wheel bearings may fail, causing the wheel to detach and increasing crash risk.

    Product
    CHARLES MACHINE — CHARLES MACHINE DITCH WITCH T26
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V160000·2015-03-20

    Forest River Recalls 2013-2014 Sabre Trailers Due to Brake Wiring Defect

    Forest River is recalling 2013-2014 Sabre travel trailers and fifth wheels because improperly routed brake wires may chafe, break, or short, increasing crash and fire risks.

    Product
    FOREST RIVER — FOREST RIVER SABRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V162000·2015-03-20

    GM Recalls 2015 Buick Encore and Chevrolet Trax for Tire Label Defect

    General Motors is recalling 2015 Buick Encore and Chevrolet Trax vehicles because tire placards lack rim size information, which may lead to incorrect rim replacement and increased crash risk.

    Product
    CHEVROLET — CHEVROLET, BUICK TRAX, ENCORE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V161000·2015-03-20

    Jerr-Dan Recalls 2010 Standard Duty Wreckers Due to Boom Drift Risk

    Jerr-Dan is recalling 50 model year 2010 Standard Duty Wreckers because the underlift boom may drift down during towing, increasing the risk of a crash.

    Product
    JERR-DAN — JERR-DAN STANDARD DUTY WRECKER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·15102·2015-03-19

    Residential Elevators Recalled Due to Crushing Hazard and Brain Injury

    CPSC recalls Elmira Hydraulic residential elevators sold by Coastal Carolina Elevators because the gate door can open while operating, causing a crushing hazard.

    Product
    Residential hydraulic elevators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V156000·2015-03-18

    Forest River Recalls 2014 Palomino SolAire Trailers Due to Furnace Vent Defect

    Forest River is recalling 2014 Palomino SolAire trailers manufactured between July and August 2014 because they may lack an exterior furnace vent, posing risks of carbon monoxide poisoning and fire.

    Product
    FOREST RIVER — FOREST RIVER PALOMINO SOLAIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1247-2015·2015-03-18

    Arjo Pressure IQ Evolve Mattress Recalled for Pressure Ulcer Risk

    Arjo is recalling 1,034 Pressure IQ Evolve mattresses nationwide due to failures that resulted in pressure ulcers.

    Product
    Pressure IQ Evolve Mattress; Non-powered mattress replacement system. Intended for patients with medium to high risk for developing pressure ulcers while on a mattress.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V157000·2015-03-18

    GM Recalls 2015 Chevrolet Colorado and GMC Canyon for Air Bag Defect

    General Motors is recalling 2015 Chevrolet Colorado and GMC Canyon vehicles because the driver's air bag inflator may be misaligned, posing a risk of injury during deployment.

    Product
    CHEVROLET — CHEVROLET, GMC COLORADO, CANYON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1256-2015·2015-03-18

    Siemens Healthcare Recalls Capillary Caps Due to Breakage Risk

    Siemens Healthcare is recalling capillary caps for RAPIDLyte blood collection devices because they may not attach properly, causing glass capillaries to break.

    Product
    Siemens Healthcare Caps for capillary 100 uL , Package count 200 For use with blood collection Multicap glass and Multicap-S plastic capillaries SMN: 10311053 Legacy Part number: 478601
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1248-2015·2015-03-18

    GE Healthcare Recalls Proteus XR/a X-ray Systems Due to Cable Breakage Risk

    GE Healthcare is recalling Proteus XR/a X-ray systems because a steel cable supporting the bucky device may break. A falling bucky could injure a patient or operator.

    Product
    GE Healthcare Proteus XR/a with wall stand model number 2260354. Intended for use in generating radiographic images of human anatomy in all general purpose diagnostic procedures. This device is not intended for mammographic applications.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1267-2015·2015-03-18

    Siemens CT System Recalled for Image Artifacts and Safety Issues

    Siemens Medical Solutions is recalling 12 SOMATOM Force CT systems due to potential image artifacts and safety-related software issues.

    Product
    SIEMENS SOMATOM Force with software version VA50A and /or VA50A_FP1 and/or VA50A_SP0; Computed tomography system. Product Usage: The intended use of computed tomography is to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1258-2015·2015-03-18

    Siemens Healthcare Recalls Capillary Caps Due to Breakage Risk

    Siemens Healthcare is recalling capillary caps that may fail to attach, causing glass capillaries to break.

    Product
    Siemens Healthcare Caps for capillary 50/60 uL, Package count 200 For use with blood collection Multicap glass and Multicap-S plastic capillaries SMN: 10328655 Legacy Part number: 478527
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1260-2015·2015-03-18

    Synthes Inserter for Titanium Elastic Nails Recalled for Mechanical Failure

    Synthes, Inc. is recalling Inserter for Titanium Elastic Nails due to potential mechanical failures including shaft breakage and chuck malfunction.

    Product
    Synthes Inserter for Titanium Elastic Nails; The Inserter for Titanium Elastic Nails (TEN) is intended for fixation of diaphyseal fractures where the canal is narrow or flexibility of the implant is paramount. This includes: lower extremity fractures in pediatric and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15E022000·2015-03-18

    Woodstock Stop Arms Recalled for Non-Compliant Border Width

    Woodstock Safety Mirror Co. is recalling specific Stop Arms because the border width is too narrow, reducing visibility and failing federal safety standards.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1261-2015·2015-03-18

    Dako Automated Slide Stainers Recalled for Potential Diagnostic Errors

    Dako North America Inc. is recalling four models of automated slide stainers because a defect may cause buffer leakage, leading to false negative diagnostic results.

    Product
    Autostainer Link 48 (AS480), Autostainer Plus Link Instrument (AS100), Autostainer (S3400), and Autostainer Plus (S3800). Automated slide stainer for in vitro diagnostic use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V158000·2015-03-18

    Charles Machine Recalls Ditch Witch T18 Trailers Due to Wheel Lockup Risk

    Charles Machine is recalling 2013-2015 Ditch Witch T18 trailers because incorrect bearing pre-loads may cause wheels to lock up, increasing crash risk.

    Product
    CHARLES MACHINE — CHARLES MACHINE DITCH WITCH T18
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1257-2015·2015-03-18

    Siemens Healthcare Recalls Capillary Caps Due to Breakage Risk

    Siemens Healthcare is recalling capillary caps that may fail to attach, causing glass capillaries to break.

    Product
    Siemens Healthcare Caps for capillary 140/175 uL, Package count 100 For use with blood collection Multicap glass and Multicap-S plastic capillaries SMN: 10311054 Legacy Part number: 478605
    Category
    Medical Device
    Distribution
    Distributed nationwide