The Recall Desk

State

Northern Mariana Islands product recalls

73,597 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 73,597 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29201–29225 of 73620

  • ModerateFDA (Drugs)·D-1229-2020·2020-04-22

    Aurobindo Recalls Acetaminophen and Codeine Tablets Due to Water Leakage

    Aurobindo Pharma USA Inc. is recalling specific lots of Acetaminophen and Codeine Phosphate tablets because they were manufactured in an area with observed water leakage.

    Product
    ACETAMINOPHEN AND CODEINE PHOSPHATE — ACETAMINOPHEN AND CODEINE PHOSPHATE (ACETAMINOPHEN AND CODEINE PHOSPHATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1697-2020·2020-04-22

    Boston Scientific Recalls Nitinol Thermocouple Electrodes Due to Incorrect Instructions

    Boston Scientific is voluntarily correcting 40 units of Nitinol Thermocouple Electrodes because they were packaged with an incorrect revision of the Instructions for Use.

    Product
    Nitinol Thermocouple Electrode, 15 cm, 3m Cable - Product Usage: The TCN Electrode is indicated for use in RF heat lesioning of peripheral nerve tissue only.The Cosman Medical TCN Electrodes are temperature-sensing probes for use in the percutaneous treatment of pain.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1230-2020·2020-04-22

    Aurobindo Recalls Acetaminophen and Codeine Tablets Due to Manufacturing Deviations

    Aurobindo Pharma USA Inc. is recalling specific lots of Acetaminophen and Codeine Phosphate tablets because they were manufactured in an area with observed water leakage.

    Product
    ACETAMINOPHEN AND CODEINE PHOSPHATE — ACETAMINOPHEN AND CODEINE PHOSPHATE (ACETAMINOPHEN AND CODEINE PHOSPHATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1706-2020·2020-04-22

    Life Technologies Recalls Oncomine Dx Target Test Due to Expiration Date Error

    Life Technologies is recalling 35 units of the Oncomine Dx Target Test because the expiration date was extended prior to clearance.

    Product
    Oncomine Dx Target Test RNA/DNA Panel- IVD for detection of DNA and RNA isolated from non-small cell lung cancer (NSCLC) tumor specimens, Catalog Number: A32441
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1707-2020·2020-04-22

    Life Technologies Recalls Ion Torrent Dx No Template Control Kit

    Life Technologies is recalling 79 units of the Ion Torrent Dx No Template Control Kit due to extended expiration dates prior to clearance.

    Product
    Ion Torrent Dx No Template Control Kit- IVD for detection of DNA and RNA isolated from non-small cell lung cancer (NSCLC) tumor specimens Catalog Number: A32444
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1231-2020·2020-04-22

    Aurobindo Recalls Acetaminophen and Codeine Tablets Due to Water Leakage

    Aurobindo Pharma USA Inc. is recalling specific lots of Acetaminophen and Codeine Phosphate tablets because they were manufactured in an area with observed water leakage.

    Product
    ACETAMINOPHEN AND CODEINE PHOSPHATE — ACETAMINOPHEN AND CODEINE PHOSPHATE (ACETAMINOPHEN AND CODEINE PHOSPHATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1705-2020·2020-04-22

    Life Technologies Recalls Oncomine Dx Target Test RNA Control for Expiration Date Error

    Life Technologies is recalling 66 units of the Oncomine Dx Target Test RNA Control because the expiration date was extended prior to regulatory clearance.

    Product
    Oncomine Dx Target Test RNA Control- IVD for detection of DNA and RNA isolated from non-small cell lung cancer (NSCLC) tumor specimens, Catalog Number: A32443
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1237-2020·2020-04-22

    Aurobindo Recalls Oxycodone and Acetaminophen Tablets Due to Water Leakage

    Aurobindo Pharma USA Inc. is recalling specific lots of Oxycodone and Acetaminophen tablets because they were manufactured in an area with observed water leakage.

    Product
    OXYCODONE AND ACETAMINOPHEN — OXYCODONE AND ACETAMINOPHEN (OXYCODONE AND ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1695-2020·2020-04-22

    Boston Scientific Recalls Nitinol Thermocouple Electrodes Due to Incorrect Instructions

    Boston Scientific is voluntarily recalling 110 Nitinol Thermocouple Electrodes because they were packaged with incorrect Instructions for Use.

    Product
    Nitinol Thermocouple Electrode, 10 cm, 3m Cable - Product Usage: The TCN Electrode is indicated for use in RF heat lesioning of peripheral nerve tissue only.The Cosman Medical TCN Electrodes are temperature-sensing probes for use in the percutaneous treatment of pain.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1694-2020·2020-04-22

    Boston Scientific Recalls Nitinol Thermocouple Electrodes Due to Incorrect Instructions

    Boston Scientific is voluntarily correcting 437 units of Nitinol Thermocouple Electrodes because they were packaged with an incorrect revision of the Instructions for Use.

    Product
    Nitinol Thermocouple Electrode, 10 cm - Product Usage: The TCN Electrode is indicated for use in RF heat lesioning of peripheral nerve tissue only.The Cosman Medical TCN Electrodes are temperature-sensing probes for use in the percutaneous treatment of pain.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V225000·2020-04-21

    Altec Recalls 2017-2020 ST Spray Trucks Due to Electrical Fire Risk

    Altec is recalling 92 ST Spray Trucks from 2017-2020 because an improperly mounted battery fuse holder may cause an electrical short circuit and fire.

    Product
    ALTEC — ALTEC ST SPRAY TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V227000·2020-04-21

    Mercedes-Benz Recalls 2020 AMG GT for eCall Wiring Defect

    Mercedes-Benz is recalling 2020 AMG GT vehicles because a missing wiring ground line may cause the emergency call system to relay inaccurate location data or prevent verbal communication with the call center.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V228000·2020-04-21

    Mercedes-Benz Recalls 2020 E 450 Coupe for Front Seatbelt Webbing Damage

    Mercedes-Benz is recalling 2020 E 450 Coupe vehicles because the front left seatbelt may contact sharp metal components, potentially damaging the webbing and reducing crash protection.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V223000·2020-04-20

    Eldorado CNG Vehicles Recalled for Fuel System Rupture Risk

    Eldorado is recalling 2018-2020 CNG-powered vehicles because the pressure relief device may fail to vent heat, potentially causing the fuel system to rupture.

    Product
    ELDORADO — ELDORADO XHF, E-Z RIDER II, AXESS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V222000·2020-04-20

    TransitWorks Recalls Driverge Vans for Seat Belt Retract Issues

    TransitWorks is recalling 2019-2020 Ford Transit and RAM ProMaster vans because seat belt retractors may not secure occupants properly.

    Product
    RAM — RAM, FORD PROMASTER, TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V219000·2020-04-17

    International DuraStar and WorkStar Fuel Heater Fire and Engine Stall Recall

    Navistar is recalling 2017-2020 International DuraStar and WorkStar models, plus IC bus vehicles with Cummins B6.7 engines. The electric fuel heater may overheat and catch fire or cause engine stalling.

    Product
    IC BUS — IC BUS, INTERNATIONAL TC, CE, MV, DURASTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·20733·2020-04-16

    Polaris Recalls 2018-2020 Ranger XP 1000 Off-Road Vehicles Due to Fire Hazard

    Polaris is recalling approximately 80,000 Model Year 2018-2020 Ranger XP 1000 and CREW XP 1000 off-road vehicles because a broken clutch belt can damage the fuel line and cause a fire.

    Product
    Model Year 2018 - 2020 Ranger XP 1000 & CREW XP 1000 Off-Road Vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V218000·2020-04-16

    Subaru Recalls 2019 Models for Fuel Pump Failure Risk

    Subaru is recalling 2019 Impreza, Outback, Legacy, and Ascent vehicles because the low pressure fuel pump may fail, causing the engine to stall.

    Product
    SUBARU — SUBARU IMPREZA, LEGACY, ASCENT, OUTBACK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20734·2020-04-16

    Polaris Recalls 2019-2020 Ranger XP 1000 Off-Road Vehicles Due to Fire Hazard

    Polaris is recalling approximately 7,000 Model Year 2019-2020 Ranger XP 1000 and CREW XP 1000 off-road vehicles because a misrouted fuel line poses a fire hazard.

    Product
    Model Year 2019 - 2020 Ranger XP 1000 & CREW XP 1000 Off-Road Vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide