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.

56726–56750 of 73850

  • ModerateFDA (Devices)·Z-2723-2014·2014-10-08

    Instrumed Reusable Laparoscopic Instruments Recalled for Updated Caution Statements

    Instrumed International is recalling 156 reusable laparoscopic instruments to add caution statements regarding voltage limits and useful life to the Instructions For Use.

    Product
    Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior to use. The instruments are intended to be used by qualified physicians to provide access, illumination and visualization of internal structures and for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2725-2014·2014-10-08

    Instrumed Reusable Laparoscopic Instruments Recalled for Updated Safety Instructions

    Instrumed International is recalling 83 reusable laparoscopic instruments to add caution statements regarding voltage limits and product useful life.

    Product
    Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior to use. The instruments are intended to be used by qualified physicians to provide access, illumination and visualization of internal structures and for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0009-2015·2014-10-08

    Gendex eXpertDC Intraoral X-Ray Recall for Spring Link Failures

    Gendex Corp is recalling 651 eXpertDC intraoral x-ray units worldwide because spring link components in the articulated arm assembly broke during normal assembly.

    Product
    eXpertDC intraoral x-ray, models: eXpert DC, NA, 75 Inch reach; eXpert DC, NA, 65 Inch reach; eXpert DC, CN, 55 Inch reach; eXpert DC, WW, 75 Inch reach; eXpert DC, WW, 65 Inch reach; eXpert DC, WW, 55 Inch reach; OEM Arm Assembly w/o cables; Assy, Articulated Arm & Tubehead…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2736-2014·2014-10-08

    Nanosphere Recalls Verigene BC-GN Kits Due to Processing Error Risk

    Nanosphere is recalling Verigene BC-GN Kits because a specific lot of extraction trays may cause processing errors in the device.

    Product
    Verigene BC-GN Kit (Catalog number 20-005-021); 1) 20 Verigene BC-GN Test Cartridges; are qualitative multiplexed in vitro diagnostic tests for simultaneous detection and identification of selected gram-positive (BC-GP) and gram-negative (BC-GN) bacteria and resistance markers.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0007-2015·2014-10-08

    Ortho-Clinical Diagnostics Recalls VITROS Phenytoin Slides Due to Potential Bias

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products PHYT Slides because they may produce biased results, potentially affecting patient care.

    Product
    VITROS Chemistry Products PHYT (Phenytoin) Slides, REF/Product Code 829 8671, IVD. For in vitro diagnostic use only. VITROS Chemistry Products PHYT Slides quantitatively measure phenytoin (PHYT) concentration in serum and plasma using VITROS 250/350/950/5,1 FS and 4600…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2729-2014·2014-10-08

    Instrumed Reusable Laparoscopic Instruments Recalled for Updated Safety Instructions

    Instrumed International is recalling 15 reusable laparoscopic instruments to add caution statements regarding voltage limits and product life to the Instructions For Use.

    Product
    Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior to use. The instruments are intended to be used by qualified physicians to provide access, illumination and visualization of internal structures and for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2735-2014·2014-10-08

    Nanosphere Verigene BC-GP Kit Extraction Tray Recall

    Nanosphere is recalling Verigene BC-GP Kit extraction trays because a specific lot may cause processing errors and tips to drop into the processor.

    Product
    Verigene BC-GP Kit (Catalog number 20-005-018); 1) 20 Verigene BC-GP Test Cartridges; are qualitative multiplexed in vitro diagnostic tests for simultaneous detection and identification of selected gram-positive (BC-GP) and gram-negative (BC-GN) bacteria and resistance markers.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0010-2015·2014-10-08

    GE Healthcare Precision 500D X-ray Systems Recalled for Missing Screws

    GE Healthcare is recalling Precision 500D X-ray systems because missing screws may cause the overhead video monitor to detach from the tray assembly.

    Product
    GE Healthcare Precision 500D, Classical R&F System. Product Usage: The Precision 500D R&F X-ray System is intended to be used as a universal diagnostic imaging system for radiographic and fluoroscopic examinations, including general R&F and Pediatric examinations.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2722-2014·2014-10-08

    Instrumed Reusable Laparoscopic Instruments Recalled for Updated Safety Instructions

    Instrumed International is recalling reusable laparoscopic instruments to add caution statements regarding voltage limits and product life.

    Product
    Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior to use. The instruments are intended to be used by qualified physicians to provide access, illumination and visualization of internal structures and for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2721-2014·2014-10-08

    Instrumed Reusable Laparoscopic Instruments Recalled for Updated Safety Instructions

    Instrumed International is recalling 65 reusable laparoscopic instruments to add caution statements regarding voltage limits and useful life to the Instructions For Use.

    Product
    Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior to use. The instruments are intended to be used by qualified physicians to provide access, illumination and visualization of internal structures and for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1617-2014·2014-10-08

    Actavis Recalls Diclofenac Sodium and Misoprostol Tablets Due to Splitting

    Actavis is recalling 6,041 bottles of Diclofenac Sodium and Misoprostol tablets because they may be split or broken.

    Product
    DICLOFENAC SODIUM AND MISOPROSTOL — DICLOFENAC SODIUM AND MISOPROSTOL (DICLOFENAC SODIUM AND MISOPROSTOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2726-2014·2014-10-08

    Instrumed Reusable Laparoscopic Instruments Recalled for Updated Safety Instructions

    Instrumed International is recalling 122 reusable laparoscopic instruments to add caution statements regarding voltage limits and product life to the Instructions For Use.

    Product
    Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and sterilization of devices must occur prior to use. The instruments are intended to be used by qualified physicians to provide access, illumination and visualization of internal structures and for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2717-2014·2014-10-08

    KCI CelluTome Epidermal Harvesting System Recalled Due to Blade Shift

    KCI USA, Inc. is recalling 1,331 units of the CelluTome Epidermal Harvesting System because the blade can shift during shipping, rendering the product ineffective.

    Product
    CelluTome Epidermal Harvesting System Part number CT-H25 or Part Number CT-H50
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V626000·2014-10-07

    EZ Loader Recalls 2014-2015 Adjustable Steel and Aluminum Trailers

    EZ Loader is recalling 1,357 model year 2014-2015 Adjustable Steel and Aluminum trailers because a suspension bar may break, increasing crash risk.

    Product
    EZ LOADER — EZ LOADER ADJUSTABLE ALUM TRAILER, ADJUSTABLE STEEL TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V629000·2014-10-07

    Suzuki Recalls GSX-R Motorcycles Due to Drive Chain Adjuster Defect

    Suzuki is recalling 2009-2014 GSX-R1000 and 2011-2014 GSX-R750 motorcycles because a damaged drive chain adjuster could cause the chain to come off, increasing crash risk.

    Product
    SUZUKI — SUZUKI GSX-R1000, GSX-R750
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V627000·2014-10-07

    BMW Recalls 2012-2014 Models for Brake Vacuum Pump Defect

    BMW is recalling specific 2012-2014 models because a vacuum pump may fail due to insufficient lubrication, reducing braking power and increasing crash risk.

    Product
    BMW — BMW X1 SAV, 528I, 320I, 328I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V625000·2014-10-07

    Forest River Recalls 2014-2015 Salem and Wildwood RVs for Label Errors

    Forest River is recalling 2014-2015 Salem and Wildwood recreational vehicles because incorrect weight labels may lead to tire failure and crashes.

    Product
    FOREST RIVER — FOREST RIVER SALEM, WILDWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15701·2014-10-07

    KYMCO Recalls MXU 700 ATVs Due to Fuel Tank Fire and Burn Hazards

    KYMCO is recalling approximately 540 MXU 700 ATVs from model years 2013 to 2015 because fuel tank pressure buildup can cause ruptures, fires, or burns.

    Product
    All-terrain vehicles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V628000·2014-10-07

    Trans Tech School Buses Recalled for Wheelchair Lift Platform Cracking

    Trans Tech is recalling 188 school buses equipped with Ricon wheelchair lifts because the platform side plates may crack, posing an injury risk to operators.

    Product
    TRANS TECH — TRANS TECH STUDENT SAFETY TRANSPORT, ROADSTAR, STUDENT TRANSPORTER AERO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V622000·2014-10-06

    Micro Bird Transit Bus Recall for Wheelchair Lift Platform Cracking

    Micro Bird is recalling 2006-2014 MB II and G5 transit buses because wheelchair lift platform side plates may crack, posing an injury risk.

    Product
    MICRO BIRD — MICRO BIRD MB II TRANSIT BUS, G5 TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V624000·2014-10-06

    GM Recalls 2015 Cadillac Escalade Models for Air Bag Defect

    General Motors is recalling 2015 Cadillac Escalade and Escalade ESV vehicles because a manufacturing defect may cause inconsistent passenger air bag deployment.

    Product
    CADILLAC — CADILLAC ESCALADE, ESCALADE ESV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V621000·2014-10-06

    Micro Bird Recalls School Buses with Cracking Wheelchair Lifts

    Micro Bird is recalling 2006-2014 school buses equipped with specific Ricon wheelchair lifts because the platform side plates may crack, posing an injury risk.

    Product
    MICRO BIRD — MICRO BIRD MB II SCHOOL BUS, G5 SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V623000·2014-10-06

    Spartan Emergency Vehicles Recalled for Transmission Fluid Cooler Failure

    Spartan is recalling 2006-2013 emergency vehicles because a failing transmission fluid cooler may allow engine coolant to mix with transmission fluid, increasing crash risk.

    Product
    SPARTAN — SPARTAN METROSTAR, ADVANTAGE, GLADIATOR, DIAMOND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V619000·2014-10-03

    BMW Recalls 2014 MINI Cooper Hardtop for Spare Wheel Nut Defect

    BMW is recalling 2014 MINI Cooper Hardtop vehicles because the spare wheel nut may not be self-locking. This could allow the wheel to separate from the vehicle, creating a road hazard.

    Product
    MINI — MINI COOPER
    Category
    Vehicle
    Distribution
    Distributed nationwide