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.

57226–57250 of 73856

  • HighFDA (Drugs)·D-1576-2014·2014-09-10

    Apotex Recalls Paroxetine Hydrochloride Tablets Due to Chemical Contamination

    Apotex Inc. is recalling Paroxetine Hydrochloride Controlled-Release Tablets 25 mg because they were manufactured with active pharmaceutical ingredient batches contaminated with residual materials and solvents.

    Product
    PAROXETINE HYDROCHLORIDE — PAROXETINE HYDROCHLORIDE (PAROXETINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2560-2014·2014-09-10

    OrthoPediatrics ACL Sleeve Installation Tool Recalled for Weld Fractures

    OrthoPediatrics Corp is recalling 56 ACL Sleeve Installation Tools due to weld fractures. The tools are used in pediatric and small stature adult ACL reconstruction systems.

    Product
    ACL Sleeve Installation Tool Sizes: 6mm, 6.5mm, 7.0mm, 7.5mm, 8.0mm, 8.5mm, 9.0mm, 10.0mm Product Usage: The OrthoPediatrics ACL Reconstruction System is a pediatric and small stature adult ACL reconstruction system that offers both the fixation devices and instrument in one…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2561-2014·2014-09-10

    Siemens EasyLink Informatics System Recall for Potential Result Transmission Errors

    Siemens Healthcare Diagnostics is recalling the EasyLink Informatics System V4.0/V5 because it may release results to the Laboratory Information System that should have been held for manual review.

    Product
    Siemens EasyLink Informatics System V4.0/V5 Siemens, Material Number (SMN) 10444799, 10444800, 10487219 A clinical data management system that assists medical laboratory professionals with preanalytic and post-analytic functions in conjunction with multiple instruments…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2591-2014·2014-09-10

    Mentor Saline Breast Implant Sizer Recalled for Volume Labeling Error

    Mentor Texas, LP. is recalling 34 units of saline breast implant sizers because the device labeling states 330cc while the actual device volume is 380cc.

    Product
    EN MENTOR Round High Profile Single Use Saline Breast Implant Sizer Single Use Saline Breast Implant Sizer REF 351-3380SZ 380 cc LOT 6830722. Product Usage: This product is indicated for single use for temporary insertion intraoperatively to evaluate the volume of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1572-2014·2014-09-10

    Qualitest Recalls Oxycodone and Acetaminophen Tablets Due to Broken Tablets

    Qualitest Pharmaceuticals is recalling 23,544 bottles of Oxycodone and Acetaminophen tablets because broken tablets were found in sealed bottles.

    Product
    OXYCODONE and ACETAMINOPHEN, USP 10 mg/325 mg, CII, 100 TABLETS, Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811, NDC 0603-4982-21
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2571-2014·2014-09-10

    Siemens Recalls V5Ms Transesophageal Ultrasound Transducers Due to Material Deterioration

    Siemens is recalling 321 V5Ms transesophageal ultrasound transducers because the material covering the articulating section has deteriorated.

    Product
    V5Ms Transesophageal transducers; V5Ms trans-esophageal echocardiograph (TEE) ultrasound transducer is intended primarily for cardiology applications
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2592-2014·2014-09-10

    MedComp Recalls Split Cath III Trays Due to Incorrect Length Labeling

    Medical Components, Inc. is recalling 110 Split Cath III Trays because they were incorrectly labeled as 32CM instead of 28CM.

    Product
    Split Cath III Trays, 16F x 28CM Product Usage: The Split Cath III is indicated for use in attaining long term vascular access for hemodialysis and apheresis in adult patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V541000·2014-09-09

    GM Recalls 2013-2015 Cadillac XTS and Chevrolet Impala for Brake Fire Risk

    General Motors is recalling 2013-2015 Cadillac XTS and 2014-2015 Chevrolet Impala vehicles because the electronic parking brake may not fully retract, potentially causing a fire.

    Product
    CHEVROLET — CHEVROLET, CADILLAC IMPALA, XTS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V543000·2014-09-09

    GM Recalls 2014 Chevrolet Sonic Vehicles for Air Bag Defect

    General Motors is recalling 2014 Chevrolet Sonic vehicles because a steering column electrical issue may limit air bag deployment in severe crashes.

    Product
    CHEVROLET — CHEVROLET SONIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V542000·2014-09-09

    GM Recalls 2004-2007 Cadillac CTS-V and STS-V for Fuel Pump Fire Risk

    General Motors is recalling specific 2004-2007 Cadillac CTS-V and STS-V vehicles because fuel pump terminals may overheat, melt, and leak fuel, increasing the risk of stalling or fire.

    Product
    CADILLAC — CADILLAC CTS, STS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V540000·2014-09-09

    GM Recalls 2008-2013 Vehicles for Ignition Key Knee Interference Risk

    General Motors is recalling 2008-2009 Pontiac G8 and 2011-2013 Chevrolet Caprice vehicles because the driver's knee may accidentally knock the ignition key out of the run position, potentially disabling safety systems.

    Product
    PONTIAC — PONTIAC, CHEVROLET G8, CAPRICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14E060000·2014-09-09

    Clean Fuel USA Recalls LPI Fuel Rails for Propane Leak Risk

    Clean Fuel USA is recalling specific LPI fuel rails for 6 and 8-liter engines because improperly secured injectors or leaking tubes may cause a propane leak, leading to stalling or fire.

    Product
    FUEL SYSTEM, OTHER:DELIVERY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14271·2014-09-09

    Cabrinha Recalls Kiteboarding Control Systems Due to Spring Jamming Risk

    Cabrinha is recalling 1X and Overdrive 1X kiteboarding control systems because the Recoil spring can jam, causing loss of control and injury risk.

    Product
    Cabrinha Kiteboarding 1X and Overdrive 1X Control Systems
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V536000·2014-09-05

    Harley-Davidson Recalls 2015 XG500 and XG750 Motorcycles for Fuel Leak Risk

    Harley-Davidson is recalling 2015 XG500 and XG750 motorcycles because the fuel tank filler neck may not seal properly, creating a risk of fuel leaks and vehicle fire.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON XG750, XG500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V537000·2014-09-05

    Harley-Davidson Recalls 2014 Motorcycles Due to Clutch Master Cylinder Defect

    Harley-Davidson is recalling 105,746 model year 2014 motorcycles because a clutch master cylinder component may fail, causing the bike to creep forward.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON FXSBSE, FLHTCUTG, FLHX, FLHRSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V538000·2014-09-04

    Jet Company Recalls 2014 Side Dump Trailers Due to Suspension Bolt Failure

    Jet Company is recalling 84 model year 2014 Side Dump Trailers because suspension pivot bolts may fail, potentially causing the axle to separate and increasing crash risk.

    Product
    JET COMPANY — JET COMPANY SIDE DUMP TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V529000·2014-09-04

    Chrysler Recalls 2013-2014 SRT Viper for Air Bag Deployment Defect

    Chrysler is recalling 2013-2014 SRT Vipers because inaccurate seat sensors may cause air bags to deploy at lower-than-designed velocities, increasing injury risk.

    Product
    SRT — SRT VIPER
    Category
    Vehicle
    Distribution
    Distributed nationwide