The Recall Desk

State

Northern Mariana Islands product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

38926–38950 of 73764

  • HighNHTSA·18V223000·2018-04-09

    MCI Recalls 2018 J4500 Coaches Due to Taillight Wiring Defect

    Motor Coach Industries is recalling 2018 J4500 vehicles because a wiring harness may contact the coolant tank, causing the left taillight to fail and reducing visibility.

    Product
    MCI — MCI J4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E022000·2018-04-06

    Keystone Recalls Husky Fifth Wheel Trailer Hitches Due to Fastener Loosening

    Keystone is recalling specific Husky fifth wheel trailer hitches because fasteners may loosen, potentially causing the jaws to open unexpectedly and increasing crash risk.

    Product
    TRAILER HITCHES:FIFTH WHEEL ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V222000·2018-04-06

    Forest River Surveyor Recalled for Incorrect Federal Tire Placard Information

    Forest River is recalling 2018 Surveyor recreational trailers because the Federal Placard lists incorrect tire sizes and pressures, which could lead to over-inflation and increased crash risk.

    Product
    FOREST RIVER — FOREST RIVER SURVEYOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E018000·2018-04-05

    Brembo Motorcycle Front Brake Master Cylinders Recalled for Piston Cracking

    Brembo is recalling specific motorcycle front brake master cylinders because the internal piston may crack and fail, potentially causing a loss of front braking ability.

    Product
    SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:MASTER CYLINDER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V219000·2018-04-05

    Newmar Recalls 2018-2019 New Aire Motorhomes Due to Valve Stem Defect

    Newmar is recalling 2018-2019 New Aire motorhomes because a wheel valve stem stabilizer may dislodge, potentially causing tire damage and increasing crash risk.

    Product
    NEWMAR — NEWMAR NEW AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V221000·2018-04-05

    Honda Recalls 2018 Pilot, Ridgeline, and Acura MDX for Seat Rivet Defect

    Honda is recalling 2018 Pilot, Ridgeline, and Acura MDX vehicles because improperly manufactured seat rivets may break in a crash, increasing injury risk.

    Product
    HONDA — HONDA, ACURA RIDGELINE, PILOT, MDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V220000·2018-04-05

    Mitsubishi Recalls 2004-2006 Lancers for Air Bag Inflator Defect

    Mitsubishi is recalling 2004-2006 Lancers because passenger air bag inflators may explode during deployment, potentially causing serious injury or death.

    Product
    MITSUBISHI — MITSUBISHI LANCER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V218000·2018-04-05

    Doepker Recalls 2015-2016 Flatdeck Semi Trailers Due to Frame Cracking

    Doepker is recalling 2015-2016 53-foot Tridem Galvanized Highboy Flatdeck Semi trailers because lower rail main beam flanges may crack, potentially causing loads to shift and spill onto the road.

    Product
    DOEPKER — DOEPKER HG FLATDECK SEMI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1275-2018·2018-04-04

    Ray Station Software Recalled for Potential Incorrect Radiation Treatment Volume

    RaySearch Laboratories is recalling Ray Station 4.9 through 7 software due to a defect that may result in incorrect treatment volumes being delivered to patients.

    Product
    Ray Station 4.9 Ray Station 5, Ray Station 6 and Ray Station 7 Software build numbers: 4.9.0.42, 5.0.0.37, 5.0.1.11, 5.0.2.35, 6.0.0.24, 6.1.0.26, 6.1.1.2, 6.2.0.7 or 7.0.0.19 UDI: 0735000201006820171130
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1262-2018·2018-04-04

    Allen Medical Systems Recalls F-T3SYSTEM Surgical Table Accessories

    Allen Medical Systems is recalling 83 F-T3SYSTEM surgical table accessories because rail section clamps may fail during use, posing a risk of critical harm to patients.

    Product
    F-T3SYSTEM, T3 (Trumpf Table Top) System The device is a surgical table accessory system used to allow prone positioning on OR table tops during spinal surgery. The system consists of a table top frame, arm supports,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1260-2018·2018-04-04

    Encore Medical Recalls Altivate Anatomic Pegged Glenoid Trial Instruments

    Encore Medical is recalling 93 units of Altivate Anatomic Pegged Glenoid Trials because the peg base design is larger on the trials than on the implants.

    Product
    Altivate Anatomic(TM) INSTRUMENTATION, PEGGED GLENOID TRIAL, SIZE 54mm, REF 804-07-540 Product Usage: The AltiVate Anatomic Shoulder System is a total shoulder system indicated as an anatomic shoulder joint replacement for patients suffering from pain and dysfunction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V213000·2018-04-04

    Ford Recalls 2017-2018 Vehicles for Missing Transmission Roll Pin

    Ford is recalling 2017-2018 F-150, Expedition, Mustang, and Navigator vehicles because a missing transmission roll pin may cause the vehicle to roll away from Park.

    Product
    LINCOLN — LINCOLN, FORD NAVIGATOR, MUSTANG, EXPEDITION, F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0978-2018·2018-04-04

    Piggie Park Recalls Honey BBQ Sauces Due to Undeclared Soy and Wheat

    Piggie Park Enterprises Inc. is recalling Maurice's Honey Southern Gold BBQ Sauce and Carolina Gold Honey Sauce because they contain undeclared soy and wheat ingredients.

    Product
    Maurice's Honey Southern Gold BBQ Sauce; Net Wt. 18 oz. bottles; UPC Code 0 7561654332 6 and Carolina Gold Honey Sauce; Net Wt. 18 oz. bottle; UPC Code 0 7561654383 8
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1175-2018·2018-04-04

    ConMed Mini Infant Radiotranslucent Electrodes Recalled for Adhesive Conductivity Issues

    ConMed is recalling 18,720 Mini Infant Radiotranslucent Electrodes because adhesive on contact wires may impede conductivity and cause failure.

    Product
    MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, Philips Plug Style Connector, REF/Catalog Number 2602H Indicated for use in external pacing, defibrillation and monitoring applications as a non-sterile, disposable device for single pediatric use, only. The PadPro 2602…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V214000·2018-04-04

    Ford Recalls 2018 F-Series and Expedition for Gear Shift Cable Defect

    Ford is recalling 2018 F-650, F-750, F-150, and Expedition vehicles because a gear shift cable clip may not be seated, causing the transmission to be in a different gear than indicated.

    Product
    FORD — FORD EXPEDITION, F-150, F-750 SD, F-650 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V215000·2018-04-04

    Zero Motorcycles Recalls 2012 Models Due to Battery Fire Risk

    Zero Motorcycles is recalling 2012 S, DS, and DSP models because battery wear may cause electrical shorts and fire. Owners should stop riding and charging these vehicles.

    Product
    ZERO — ZERO ZERO S, ZERO DS, DSP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1236-2018·2018-04-04

    Zimmer Biomet Recalls Phoenix Nail System Inserter Connectors Due to Fracturing

    Zimmer Biomet is recalling specific lots of Phoenix Nail System 3.5mm Inserter Connectors because they have fractured and remained in the device implant.

    Product
    Phoenix Nail System, intended for use with an intramedullary nail system for alignment, stabilization and fixation of fractures. 3.5mm Inserter Connector, Short; Model Number: 14-441045; Kit Model Numbers: 14-400082, 14-400082S, 14-440065S, 14-442000-00, 14-442000S…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0610-2018·2018-04-04

    Amneal Recalls Fosphenytoin Sodium Injection Due to Particulate Matter

    Amneal Pharmaceuticals is recalling specific lots of Fosphenytoin Sodium Injection because of the presence of particulate matter.

    Product
    Fosphenytoin Sodium Injection, USP 500 mg PE*/10 mL, Made in India. Distributed by: Amneal Biosciences, Bridgewater, NJ 08807, NDC 70121-1390-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1177-2018·2018-04-04

    ConMed Pediatric Defibrillation Electrodes Recalled for Adhesive Conductivity Issues

    ConMed is recalling 18,720 pediatric defibrillation electrodes because adhesive on contact wires may impede conductivity and cause failure.

    Product
    MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, Physio-Control¿ Quik-Combo" Connector, REF/Catalog Number 2602M Indicated for use in external pacing, defibrillation and monitoring applications as a non-sterile, disposable device for single pediatric use, only. The PadPro 2602…
    Category
    Medical Device
    Distribution
    Distributed nationwide