The Recall Desk

State

Northern Mariana Islands product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

59501–59525 of 73856

  • ModerateFDA (Devices)·Z-0892-2014·2014-02-05

    Synergetics Vivid Endo Illuminator Recalled for Faulty Sterile Seals

    Synergetics Inc. is recalling Vivid Endo Illuminators because faulty seals on the outer pouch could fail, compromising the sterile status of the single-use ophthalmic devices.

    Product
    Vivid (tm) Endo Illuminator, 20ga, Synergetics, inc., length 7.5 ft, sterile / EO, 56.20P. Packed 12 units per box. Manufactured for Synergetics, Inc., O'Fallon, MO.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0900-2014·2014-02-05

    Boston Scientific Recalls 1068 Peripheral Imaging Catheters Due to Guidewire Issues

    Boston Scientific is recalling 1,068 units of the Atlantis PV 8.5F Peripheral Imaging Catheter because physicians reported an inability to pass a guidewire through the device.

    Product
    Atlantis PV, 8.5F, 15 MHz Peripheral Imaging Catheter: Sterile, R; Sterilized using irradiation. Product Usage: This catheter is a 15 MHz ultrasound imaging catheter intended to operate with an IVUS instrument for diagnostic imaging. It is used with an…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0825-2014·2014-02-05

    Siemens ACUSON SC2000 Ultrasound System Recalled for Control Panel Lock Failure

    Siemens is recalling 271 ACUSON SC2000 ultrasound systems because the control panel locking mechanism can fail, making the device difficult to steer during transport.

    Product
    ACUSON SC2000 Power Input: 100-240VAC, 1600 Max 50/60Hz; Siemens Medical Solutions USA, Inc. 685 East Middlefield Road Mountain View, CA 94043 Ultrasound imaging system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0867-2014·2014-02-05

    Siemens Free T3 Assay Kits Recalled for Positive Bias in Results

    Siemens Healthcare Diagnostics is recalling Free T3 Assay kits due to a positive bias that may cause normal thyroid patients to appear abnormal.

    Product
    T3F, Free T3 Assay, REF/Catalog Number LKF31, Siemens Material Number (SMN) 10381626; an IVD Immunoassay kit for use with the IMMULITE/IMMULITE 1000 Analyzers --- Shipping or unit package: 100, 200, 500 and 600 test kits --- Origin: UK Siemens Healthcare Diagnostics Products…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0840-2014·2014-02-05

    GE Optima CT Systems Recalled for Manual Film Composer Data Mismatch

    GE Healthcare is recalling 272 Optima CT520 and CT540 systems because the Manual Film Composer feature may display or print images with incorrect patient names or mismatched image previews.

    Product
    GE Optima CT520 and Optima CT540 Computed Tomography (CT) systems. Intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0832-2014·2014-02-05

    Philips Brilliance iCT Computed Tomography Systems Recalled for Image Artifacts

    Philips is recalling seven Brilliance iCT and iCT SP CT scanners because patient images exhibited ring artifacts.

    Product
    Brilliance iCT & Brilliance iCT SP Computed Tomography X-Ray Systems, Philips Healthcare, Cleveland, OH The Brilliance iCT and iCT SP are whole body Computed Tomography X-Ray Systems intended to produce cross-sectional images of the body by computer reconstruction of x-ray…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0841-2014·2014-02-05

    BioMérieux Recalls ZYM B Reagent Due to Visual Defect and False Negatives

    BioMérieux is recalling ZYM B Reagent (REF 70493) because a visual defect and activity issue can cause false negative results in API biochemical tests.

    Product
    ZYM B Reagent (REF 70493) ZYM B reagent is an additional test used to reveal the results of some miniaturized biochemical test included in the API strips. The API product line is a standardized system combining several biochemical tests, which enables group or species…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0847-2014·2014-02-05

    Zimmer Dental Recalls Tapered Screw-Vent Implant Lot Due to Labeling Error

    Zimmer Dental is voluntarily recalling a specific lot of Tapered Screw-Vent Implants because some packages may display incorrect size information on the cap label.

    Product
    Tapered Screw-Vent Implant, MTX, 4.7mm x 11.5mm, 4.5mm Platform. Catalog Number TSVWB11, Lot 62470008. Class II, 510(k) K13227.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0843-2014·2014-02-05

    BioMérieux Recalls API NH Kits Due to ZYM B Reagent Defect

    BioMérieux is recalling API NH kits because a defect in the ZYM B reagent may cause false negative results in biochemical tests.

    Product
    API NH (REF 10400) API NH is a standardized system for the identification of Neisseria, Haemophilus (and related genera) and Moraxella catharrhalis (Branhamella catarrhalis), which uses miniaturized tests, as well as a specially adapted database. API NH also enables the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0853-2014·2014-02-05

    GE Healthcare Recalls Innova IGS 630 Biplane Imaging Systems

    GE Healthcare is recalling 28 Innova IGS 630 biplane imaging systems because a specific user action may cause the X-ray function to lock up.

    Product
    GE Healthcare Innova IGS 630. Biplane Cardiovascular and Interventional Imaging System. Product Usage: The angiographic X-ray systems are indicated for use for patients from newborn to geriatric in generating fluoroscopic and rotational images of human anatomy for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0865-2014·2014-02-05

    GE Centricity Laboratory System Software Recall for Calculation Errors

    GE Healthcare is recalling Centricity Laboratory System software due to a defect that may report calculated results as 0 or truncate them.

    Product
    The Centricity Laboratory System is intended to be an information system designed to support the clinical and administrative activities associated with the provision and utilization of clinical laboratory services and facilities, e.g., the storing and delivering of analytical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V031000·2014-02-04

    Mitsubishi Recalls 2013 Outlander Sport for Air Bag Wiring Defect

    Mitsubishi is recalling 2013 Outlander Sport vehicles with leather seats because improperly routed air bag wiring may prevent the driver's air bag from deploying in a crash.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V035000·2014-02-04

    Schwing Recalls 2012-2013 Concrete Pump Trucks Due to Fire Risk

    Schwing America is recalling 2012-2013 concrete pump trucks because a specific potting compound in DC-DC converters can conduct electricity and cause fires.

    Product
    SCHWING — SCHWING S58SX, S61SX, S39SX, S43SX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V034000·2014-02-04

    Chrysler Recalls 2014 Ram ProMaster Vehicles for Brake Hose Defect

    Chrysler is recalling 2014 Ram ProMaster vehicles because a manufacturing tool may have damaged a brake hose, potentially causing fluid leakage and reduced braking performance.

    Product
    RAM — RAM PROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V037000·2014-02-04

    Kaffenbarger Recalls International Trucks with Fire-Prone DC-DC Converters

    Kaffenbarger is recalling certain 2006-2013 International trucks because a specific DC-DC converter potting compound can conduct electricity and cause a fire.

    Product
    INTERNATIONAL — INTERNATIONAL 7600 SFA 6X4, 9900I SFA 6X4, 4300 SBA 4X2, 4300M7 SBA 4X2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V030000·2014-02-04

    Eldorado Buses Recalled for Fire Risk in Electrical Components

    Eldorado is recalling specific E-Z Rider II, Axess, and Passport buses because a potting compound in electrical components may conduct electricity and cause a fire.

    Product
    ELDORADO — ELDORADO E-Z RIDER II, AXESS, PASSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14100·2014-02-04

    Lion Force Boys' Puffer Coats Recalled for Strangulation Hazard

    Lion Force is recalling boys' puffer coats sold at Burlington Coat Factory because the hood drawstrings pose a strangulation hazard to children.

    Product
    Lion Force Boys' Puffer Coats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14099·2014-02-04

    3T Design Recalls Cervélo P5 Bicycles with Aduro Handlebars

    3T Design is recalling Cervélo P5 bicycles with Aduro aero handlebars because the forward extension mounts can detach while riding, posing a risk of injury.

    Product
    Cervélo P5 bicycles with 3T Aduro aero handlebars
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V033000·2014-02-04

    Heartland Recalls Fifth Wheel Travel Trailers Due to Incorrect Certification Label

    Heartland is recalling 2014 fifth wheel travel trailers equipped with optional 17.5-inch wheels because the Federal Certification Label contains incorrect wheel specifications.

    Product
    HEARTLAND — HEARTLAND GRAND CANYON, MONTEREY, SAN ANTONIO, SAVANNAH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·009-2014·2014-02-01

    House of Smoke Recalls Meat Products Due to Undeclared Soy Lecithin

    House of Smoke, Inc. is recalling approximately 144,000 pounds of meat and poultry products because they contain soy lecithin, a known allergen not declared on the label.

    Product
    House Of Smoke, Inc. — Colorado Firm Recalls Various Meat Products Due To Soy Lecithin
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V026000·2014-01-30

    Kenworth T370 Recall for Transmission Software Defect

    PACCAR is recalling 2014 Kenworth T370 chassis with Eaton hybrid transmissions because software may cause unintended acceleration.

    Product
    KENWORTH — KENWORTH T370
    Category
    Vehicle
    Distribution
    Distributed nationwide