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.

55176–55200 of 73850

  • ModerateFDA (Devices)·Z-1141-2015·2015-03-04

    Intuitive Surgical Recalls EndoWrist Vessel Sealers Due to Grip Interference

    Intuitive Surgical is recalling 3,282 EndoWrist One Vessel Sealers because manufacturing variability may cause interference in the instrument grips.

    Product
    EndoWrist One Vessel Sealer, IS3000, 6 pack used in conjunction with the da Vinci Surgical System Si IS3000 The EndoWrist One Vessel Sealer is a bipolar electrosurgical instrument for use with the da Vinci Surgical System and the ERBE VIO 300 D electrosurgical generator. It is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0394-2015·2015-03-04

    Sun Pharma Recalls Ketorolac Ophthalmic Solution Due to Particulate Matter

    Sun Pharma Global Fze is recalling specific bottles of Ketorolac Tromethamine Ophthalmic Solution because the product contains particulate matter exceeding specification limits.

    Product
    Ketorolac Tromethamine Ophthalmic Solution, 0.5%, 3 mL bottle, Rx only, Distributed by: Caraco Pharmaceutical Laboratories Ltd., 1150 Elijah Mccoy Drive, Detroit, MI 48202; Manufactured at: Sun Pharmaceutical Ind. Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India; NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1214-2015·2015-03-04

    GE Healthcare Recalls Centricity PACS Workstation Due to Exam Merge Failure

    GE Healthcare is recalling 128 Centricity PACS Workstation systems because a software defect may cause exam records to go missing in single Study Mode.

    Product
    The Centricity PACS Workstation is intended for use as a primary diagnostic and analysis tool for diagnostic images by trained healthcare professionals, including radiologists, physicians, technologists, clinicians and nurses. It is also intended for use as a clinical review…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1147-2015·2015-03-04

    Medtronic Neurostimulator Recall Due to Inaccurate Battery Longevity Estimates

    Medtronic is recalling specific neurostimulator models because enabling cycling at certain settings may decrease battery life and cause inaccurate longevity estimates on the programmer.

    Product
    The Medtronic, Quadripolar ITREL 3 IPG, Model 7425, is a multiprogrammable device designed for use in the Stimulation of the Central Nervous System, Peripheral Nervous System, or muscles when connected to an extension and/or lead. The Medtronic InterStim II Neurostimulator…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1142-2015·2015-03-04

    Intuitive Surgical Recalls EndoWrist Vessel Sealers Due to Grip Interference

    Intuitive Surgical is recalling EndoWrist One Vessel Sealers because manufacturing variability may cause interference in the instrument grips.

    Product
    EndoWrist One Vessel Sealer, 8MM, IS4000, 6 pack used in conjunction with the da Vinci Surgical System Xi IS4000. The EndoWrist Vessel Sealer is a bipolar electrosurgical instrument for use with the da Vinci Xi Surgical System and the ERBE VIO dV electrosurgical generator. It…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V124000·2015-03-03

    Blue Bird Recalls 2016 All American School Buses for Steering Defect

    Blue Bird is recalling 2016 All American school buses because a steering shaft clamp may contact the rubber boot, increasing steering effort and crash risk.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E014000·2015-03-03

    Ford Recalls 1,608 Steering Gears for F-250 and F-350 Trucks

    Ford is recalling 1,608 Motorcraft steering gears for 2008-2010 F-250 and F-350 trucks because they may not install properly, risking loss of steering control.

    Product
    STEERING recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15E015000·2015-03-03

    Agility LNG Fuel System Recall for Corroded Solenoid Valves

    Agility is recalling LNG fuel systems installed on heavy-duty vehicles in 22 states and D.C. because corroded solenoid valves may cause the vehicle to stall, increasing crash risk.

    Product
    FUEL SYSTEM, OTHER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15088·2015-03-03

    Dream on Me Recalls 2-in-1 Bassinet to Cradle Due to Fall Hazards

    Dream on Me is recalling 2-in-1 bassinets because wire supports can disconnect, causing fabric sides to lower and posing fall and suffocation risks.

    Product
    2-in-1 Bassinet to Cradle
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V122000·2015-03-02

    Prevost Recalls 2007-2012 Buses Due to Fuel Line Fire Risk

    Prevost is recalling 455 model year 2007-2012 buses because a missing clip allows the fuel line to rub against a coolant hose, potentially causing a leak and fire.

    Product
    PREVOST — PREVOST XLII, H3-45 VIP, X3-45, H3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V121000·2015-03-02

    Honda Recalls 2014-2015 Accord and CR-V for Engine Defect

    Honda is recalling specific 2014-2015 Accord and CR-V vehicles due to improperly torqued engine bolts that may cause power loss, oil leaks, or fire.

    Product
    HONDA — HONDA ACCORD, CR-V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V123000·2015-03-02

    Kia Recalls 2014-2015 Soul Vehicles Due to Accelerator Pedal Defect

    Kia is recalling 2014-2015 Soul and Soul electric vehicles because a section of the accelerator pedal may bend and fracture, potentially causing difficulty accelerating and increasing crash risk.

    Product
    KIA — KIA SOUL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V120000·2015-03-02

    Wheeled Coach Recalls 2010 Ambulances for Electrical System Defects

    Wheeled Coach is recalling 18 model year 2010 ambulances due to potential electrical issues that may cause loss of instrument panel functions and lighting.

    Product
    WHEELED COACH — WHEELED COACH AMBULANCE-M2 CHASSIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V119000·2015-03-02

    Prevost Motorcoach Recall for Defective Fire Extinguishers

    Prevost is recalling 291 motorcoaches because certain fire extinguishers may not fully discharge, increasing injury risk during a fire.

    Product
    PREVOST — PREVOST XLII-45, X3-45, H3-45, H3-41
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·037-2015·2015-03-01

    Oscar's Hickory House Recalls Beef Jerky Due to Processing Deviation

    Oscar's Hickory House Inc. is recalling approximately 32 pounds of beef jerky due to a processing deviation that makes the product susceptible to environmental pathogens.

    Product
    Oscar's Hickory House Inc. — Oscar's Hickory House Recalls Beef Jerky Product Due To Processing Deviation
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V113000·2015-02-27

    GM Recalls 2015 Chevrolet Cruze for Parking Brake Cable Bracket Defect

    General Motors is recalling 2015 Chevrolet Cruze vehicles because parking brake cable brackets may not be properly fastened, increasing the risk of the vehicle rolling away.

    Product
    CHEVROLET — CHEVROLET CRUZE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V114000·2015-02-27

    Dodge Charger and Challenger Recall for Fuel Leak Fire Risk

    Chrysler is recalling 2015 Dodge Charger and Challenger SRT vehicles because a fuel rail hose may leak, increasing the risk of a vehicle fire.

    Product
    DODGE — DODGE CHARGER, CHALLENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V116000·2015-02-27

    Nissan Recalls 2013-2015 Altima Vehicles for Hood Latch Defect

    Nissan is recalling 2013-2015 Altima vehicles because the secondary hood latch may fail to engage, allowing the hood to open while driving.

    Product
    NISSAN — NISSAN ALTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1035-2015·2015-02-25

    GE Healthcare MRI Systems Recalled for Potential Ferrous Object Removal Delay

    GE Healthcare is recalling MRI systems because a disconnected MRU could delay the removal of ferrous objects, posing a life-threatening injury risk.

    Product
    This correction applies to all GE Healthcare MRI systems with superconducting magnets: Discovery MR450, Discovery MR750, Signa HDx, Signa HDxt, Signa HDi, GE 1.5T Signa HDe, Optima MR360, Brivo MR355, Signa Excite-HD 1.5T & 3T, Signa Excite 1.5T HD Twinspeed, Signa Excite 1.5T…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0392-2015·2015-02-25

    Hospira Recalls Lactated Ringer's Injection Due to Confirmed Mold Particulates

    Hospira Inc. is recalling 142,644 bags of Lactated Ringer's and 5% Dextrose Injection USP due to confirmed mold particulates in the solution.

    Product
    LACTATED RINGER'S and 5% DEXTROSE Injection USP, 1000 mL, flexible containers, Rx Only, Hospira, Inc., Lake Forest, IL 600045, NDC 0409-7929-09
    Category
    Drug
    Distribution
    Distributed nationwide