The Recall Desk

State

Northern Mariana Islands product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

38076–38100 of 73761

  • ModerateFDA (Devices)·Z-2113-2018·2018-06-13

    Baxter SIGMA Spectrum Infusion Pump Instructions for Use Update

    Baxter Healthcare is updating the Instructions for Use for SIGMA Spectrum Infusion Pumps to correct a discrepancy regarding the height of secondary infusion hangers.

    Product
    Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8), infusion pump, 35700BAX2 Product Usage: The Baxter SIGMA Spectrum Infusion Pump with Master Drug Library is intended to be used for the controlled administration of fluids. These fluids may include…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2110-2018·2018-06-13

    Fresenius NaturaLyte Liquid Acid Concentrate Recalled for Mislabeled Part Numbers

    Fresenius Medical Care is recalling NaturaLyte Liquid Acid Concentrate bottles due to incorrect part number labeling.

    Product
    NaturaLyte¿ Liquid Acid Concentrate for Bicarbonate Dialysis, 3.43 Liters, Part Number: 08-3231-1 Product Usage: This concentrate is formulated to be used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2067-2018·2018-06-13

    Tosoh Tumor Marker Assay Recalled Due to Strensiq Interference

    Tosoh Bioscience is recalling ST-AIA PACK PA tumor marker assays because Asfotase Alfa (Strensiq) interferes with the tests, potentially causing inaccurate results.

    Product
    ST-AIA PACK PA; Part Number: 025263 Assay, Tumor Marker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2085-2018·2018-06-13

    Tosoh ST-AIA DHEA-S Assay Recalled Due to Strensiq Interference

    Tosoh Bioscience is recalling ST-AIA DHEA-S assays because Asfotase Alfa (Strensiq) interferes with the test, potentially causing inaccurate results.

    Product
    ST-AIA DHEA-S; Part Number: 025222 Assay, Reproductive Hormone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2083-2018·2018-06-13

    Tosoh ST-AIA PACK HCG Assay Recalled Due to Strensiq Interference

    Tosoh Bioscience Inc is recalling ST-AIA PACK HCG assays because Asfotase Alfa (Strensiq) interferes with the test, potentially causing inaccurate results.

    Product
    ST-AIA PACK ¿HCG; Part Number: 025261 Assay, Reproductive Hormone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2062-2018·2018-06-13

    Siemens ADVIA Chemistry Urea Nitrogen Reagent Recalled for Calibration Failures

    Siemens Healthcare Diagnostics is recalling ADVIA Chemistry Urea Nitrogen Reagent due to increased calibration failures that prevent the system from generating results.

    Product
    ADVIA Chemistry Urea Nitrogen Reagent (material number 10309051) for use on ADVIA 1800, 2400 and XPT Chemistry Systems
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2107-2018·2018-06-13

    MicroAire SmartRelease Endoscopic System Recalled for Incorrect Sterilization Instructions

    MicroAire is recalling SmartRelease Endoscopic Systems because the Instructions for Use contain incorrect sterilization parameters.

    Product
    MicroAire SmartRelease Endoscopic System, Endoscopic Carpal Tunnel Release, SmartRelease Handpiece, containing IFU rev. D The MicroAire Carpal Tunnel Release System is for use in patients diagnosed with carpal tunnel syndrome that is not associated with, or secondary to, any…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2112-2018·2018-06-13

    Baxter SIGMA Spectrum Infusion Pump Recall for Instructional Mismatch

    Baxter is recalling SIGMA Spectrum Infusion Pumps because the instructions for use specify a 20-inch bag drop, but the firm supplies 12.5-inch hangers.

    Product
    Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6), infusion pump, 35700BAX and 35700ABB Product Usage: The Baxter SIGMA Spectrum Infusion Pump with Master Drug Library is intended to be used for the controlled administration of fluids. These fluids may…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2080-2018·2018-06-13

    Tosoh ST-AIA PACK FT3 Assay Recalled Due to Strensiq Interference

    Tosoh Bioscience Inc is recalling ST-AIA PACK FT3 assays because Asfotase Alfa (Strensiq) interferes with the tests, potentially causing inaccurate thyroid results.

    Product
    ST-AIA PACK FT3; Part Number: 025286 Assay, Thyroid
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2061-2018·2018-06-13

    NordicNeuroLab Recalls nordicICE Software Due to Coregistration Visualization Error

    NordicNeuroLab AS is recalling 121 licenses of nordicICE v 2.3.14 because a software bug causes BOLD activation maps to be visualized without accounting for coregistration.

    Product
    nordicICE v 2.3.14 nordicICE is an image processing software package to be used by trained professionals including but not limited to physicians and medical technicians. The software runs on a standard off-the-shelf PC workstation and can be used to perform image viewing…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2115-2018·2018-06-13

    Invivo Xper Flex Cardio Physiomonitoring System Recalled for Software Defect

    Invivo Corporation is recalling Xper Flex Cardio Physiomonitoring Systems because users may inadvertently close the Full Disclosure Control Window using the ESC key.

    Product
    Xper Flex Cardio Physiomonitoring System The Xper Flex Cardio physiomonitoring system is used to facilitate invasive investigation of heart and vascular, disease when non-invasive indicators warrant such. The Xper Flex Cardio physiomonitoring system may be used to display…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2091-2018·2018-06-13

    Tosoh ST-AIA PACK Prog II Recalled Due to Strensiq Interference

    Tosoh Bioscience Inc is recalling ST-AIA PACK Prog II assays because Asfotase Alfa (Strensiq) interferes with the tests, potentially causing inaccurate results.

    Product
    ST-AIA PACK Prog II; Part Number: 025239 Assay, Reproductive Hormone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2052-2018·2018-06-13

    Hobbs Bronchial Cytology Brushes Recalled for Unauthorized Marketing

    Hobbs Medical is recalling 1,820 bronchial cytology brushes because they were marketed for uses outside their FDA clearance.

    Product
    Hobbs Bronchial Cytology Brushes, Model Number 4202; 4204; 4206 To be utilized by a trained physician and/or trained personnel through a flexible endoscope when brush cell samples are required for cytological analysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2068-2018·2018-06-13

    Tosoh ST-AIA Prostate Assay Recalled Due to Strensiq Interference

    Tosoh Bioscience is recalling ST-AIA Prostate Assay kits because the drug Strensiq can cause inaccurate test results.

    Product
    ST-AIA PACK PAP; Part Number: 025262 Assay, Prostate
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2079-2018·2018-06-13

    Tosoh ST-AIA PACK T4 Thyroid Assay Recalled Due to Interference

    Tosoh Bioscience Inc is recalling ST-AIA PACK T4 thyroid assays because Asfotase Alfa (Strensiq) interferes with the tests, potentially causing inaccurate results.

    Product
    ST-AIA PACK T4; Part Number: 025258 Assay, Thyroid
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V394000·2018-06-12

    New Flyer Transit Buses Recalled for Brake Caliper Guide Pin Defect

    New Flyer is recalling 908 urban transit buses from 2014-2017 because a brake caliper guide pin may break, reducing braking ability and increasing crash risk.

    Product
    NEW FLYER — NEW FLYER XN60, XDE60, XD60, XT60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V392000·2018-06-12

    Ford Recalls 2018 Expedition, F-150, and Navigator for Fuel Pump Defect

    Ford is recalling 2018 Expedition, F-150, and Lincoln Navigator vehicles because a fuel pump weld can fracture, causing a leak that increases fire risk.

    Product
    LINCOLN — LINCOLN, FORD NAVIGATOR, EXPEDITION, F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V391000·2018-06-12

    Lamborghini Recalls Aventador Models Due to Engine Stall Risk

    Lamborghini is recalling 2012-2018 Aventador vehicles because the engine may stall unexpectedly, increasing crash risk. Dealers will install updated software.

    Product
    LAMBORGHINI — LAMBORGHINI AVENTADOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18747·2018-06-12

    Ashley Furniture Recalls Amnon Floor Lamps Due to Burn Hazard

    Ashley Furniture is recalling Amnon floor lamps because the incorrect wattage label allows users to install bulbs that can melt the power switch, posing a burn hazard.

    Product
    Amnon floor lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18174·2018-06-12

    A&I Recalls Tractor Canopies Due To ROPS Failure Injury Hazard

    A&I is recalling about 6,200 tractor canopies in the U.S. and 265 in Canada because they may fail to protect operators in a rollover accident.

    Product
    A&I tractor canopies
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18176·2018-06-12

    Uttermost Recalls Mirrors and Wall Decor Due to Falling Hazard

    Uttermost is recalling about 17,000 mirrors and wall decor items because the hanging hardware can break, causing items to fall and injure bystanders.

    Product
    Mirrors, art and wall decor
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18177·2018-06-12

    Lorex Recalls Three Video Monitor Models Due to Battery Burn Hazard

    Lorex is recalling three video monitor models because the batteries can overheat and swell, posing a burn hazard. Consumers should stop using the monitors and contact Lorex for a refund.

    Product
    Lorex video monitors models LW2751, LW2752 and LW2962H
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V393000·2018-06-12

    KME Predator Aerial Vehicles Recalled for Tether Control Software Defect

    Kovatch Mobile Equipment is recalling 2015-2018 KME Predator Aerial emergency vehicles because the aerial platform may continue moving if the tether control is unplugged.

    Product
    KME — KME PREDATOR AERIAL, PREDATOR SS AERIAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18175·2018-06-12

    Ketra Recalls D3 Recessed Downlights Due to Electrical Shock Hazard

    Ketra is recalling about 3,400 D3 recessed downlights because incorrect wiring in the power supply connectors poses an electrical shock hazard. No injuries have been reported.

    Product
    Ketra D3 recessed downlights
    Category
    Consumer Product
    Distribution
    Distributed nationwide