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.

38801–38825 of 73764

  • ModerateFDA (Devices)·Z-1422-2018·2018-04-25

    Carefusion Recalls Jamshidi Needle Biopsy Devices Due to Packaging Integrity Concerns

    Carefusion 2200 Inc is recalling 790 units of Jamshidi Needle Biopsy devices because the integrity of the sterile packaging is potentially compromised.

    Product
    JAMSHIDI NEEDLE BIOPSY [15G X 100MM DISP, 16G X 100MM DISP, 17G X 100MM, 16G X 70MM DISP]; STERILE;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1416-2018·2018-04-25

    Terumo HX2 Temperature Management System Recall for Updated Cleaning Instructions

    Terumo is recalling HX2 Temperature Management Systems to update cooler-heater cleaning instructions. The recall affects 2,393 units distributed worldwide.

    Product
    Terumo HX2 Temperature Management System, Catalog No. 809810 The Terumo HX2 Temperature Management System is indicated for use to supply temperature regulated water to heat exchangers during open heart surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0630-2018·2018-04-25

    WipeEssentials Wet Wipes Recalled for Poor Quality Water

    Diamond Wipes International is recalling WipeEssentials Wet Wipes because they were manufactured with poor quality water.

    Product
    WipeEssentials Wet Wipes (benzalkonium chloride 0.13%), 30-count pouches, Dist. by Diamond Wipes Int'l, Inc., Chino, CA 91710, UPC 7 66670 03988 6.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1394-2018·2018-04-25

    GE Healthcare Lunar DPX Bone Density Systems Recalled for Data Errors

    GE Healthcare is recalling 43 Lunar DPX bone density systems because patient reports may be sent to hospital systems with incorrect names in the header.

    Product
    GE Healthcare Lunar: a) DPX NT, Model Numbers: LU8230, LU40338, LU42357, LU42369 b) DPX MD+, Model Numbers: LU8230, LU40338, LU40352 Provides an estimate of BMD (Bone Marrow Density) at the lumbar spine and proximal femur regions. This BMD value can then be compared to a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1383-2018·2018-04-25

    Datascope Mega Intra-Aortic Balloon Catheter Recalled for Missing Contraindications

    Datascope is recalling 2,714 Mega Intra-Aortic Balloon Catheters because the U.S. Instructions for Use are missing the Contraindications section.

    Product
    Intra-Aortic Balloon Catheter Mega 7.5FR 40cc Product Usage: The intra-aortic balloon catheter and accessories are used to provide counter pulsation therapy in the aorta, whereby balloon inflation during diastole and deflation during systole increases blood supply to the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0631-2018·2018-04-25

    Sandoz Recalls Triamterene and Hydrochlorothiazide Tablets Due to Cross-Contamination

    Sandoz Incorporated is recalling specific lots of Triamterene and Hydrochlorothiazide Tablets due to the presence of unrelated ingredients.

    Product
    Triamterene and Hydrochlorothiazide Tablets, USP, 75 mg/50 mg, 500-count bottles, Rx only, Manufactured by Sandoz, Inc., Princeton, NJ 08540, NDC 0781-5067-05.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1393-2018·2018-04-25

    GE Healthcare Lunar DPX Duo and Bravo Bone Density Software Recall

    GE Healthcare is recalling Lunar DPX Duo and Bravo bone density scanners because a software issue may cause reports to be filed under the wrong patient name in the hospital system.

    Product
    GE Healthcare Lunar: a) DPX Duo, Model Number: LU41693 b) DPX Bravo, Model Number: LU41692 Provides an estimate of BMD (Bone Marrow Density) at the lumbar spine and proximal femur regions. This BMD value can then be compared to a reference population at the sole…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1418-2018·2018-04-25

    Terumo Sarns TCM II Recall for Updated Cleaning Instructions

    Terumo is recalling Sarns TCM II devices to update cleaning instructions. The recall covers 2,393 units distributed worldwide.

    Product
    Sarns TCM II, Catalog Numbers: 4415; 4416;164925; 164930;164935;164940 UDI 00886799000014 The Sarns TCM is indicated for controlling and monitoring patient temperature .
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1384-2018·2018-04-25

    Datascope Mega Intra-Aortic Balloon Catheter Recalled for Missing Contraindications

    Datascope is recalling 655 Mega Intra-Aortic Balloon Catheters because the U.S. Instructions For Use were missing the Contraindications section.

    Product
    Intra-Aortic Balloon Catheter Mega 7.5FR 30cc Product Usage: The intra-aortic balloon catheter and accessories are used to provide counter pulsation therapy in the aorta, whereby balloon inflation during diastole and deflation during systole increases blood supply to the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0629-2018·2018-04-25

    ACURE Clarifying Acne Towelettes Recalled for Poor Quality Water

    Diamond Wipes International is recalling ACURE clarifying acne towelettes because they were manufactured with poor quality water.

    Product
    ACURE, clarifying acne, glycolic + zinc (salicyclic acid 0.5%) towelettes, 30-count pouch, Distributed by Better Planet Brands, Fort Lauderdale, FL 33316, UPC 8 54049 00358 0.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1392-2018·2018-04-25

    Philips Ingenuity TF PET/CT Recalled for Unresponsive Acquisition Console

    Philips is recalling 12 Ingenuity TF PET/CT systems because the mass storage device may cause the acquisition console to become unresponsive, preventing image acquisition.

    Product
    Ingenuity TF PET/CT, Model No. 882442 Product Usage: The device is an integrated diagnostic X-ray Computed Tomography (CT) and Positron Emission Tomography (PET) system suitable for a wide range of diagnostic applications. The device utilizes the CT technology to obtain…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1417-2018·2018-04-25

    Terumo Sarns TCM Recall for Updated Cooler-Heater Cleaning Instructions

    Terumo is recalling Sarns TCM devices to update cleaning instructions for the cooler-heater component.

    Product
    Sarns TCM, Catalog No. 15747 The Sarns TCM is indicated for controlling and monitoring patient temperature .
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1395-2018·2018-04-25

    GE Healthcare Prodigy Ultrasound Recall for Incorrect Patient Data in Reports

    GE Healthcare is recalling Prodigy and Prodigy Advanced ultrasound systems because bone density exam reports may be sent to PACS with incorrect patient information in the DICOM header.

    Product
    GE Healthcare: a) Prodigy, Model Numbers: LU7248, LU8905, LU40427, LU40431, LU40626, LU40637, LU40626, LU40637, LU42021, LU42025, LU41730, LU41734, LU42344, LU42365 b) Prodigy Advanced, Model Numbers: LU42361, LU42397 Provides an estimate of BMD (Bone Marrow Density) at…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V260000·2018-04-24

    Hyundai Recalls 2017 Ioniq Hybrid Vehicles for Fire Risk

    Hyundai is recalling 2017 Ioniq Hybrid vehicles because a leaking oil seal may cause an electrical short, increasing the risk of a fire.

    Product
    HYUNDAI — HYUNDAI IONIQ HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18146·2018-04-24

    Honeywell Recalls Fibre-Metal E2 and North Peak A79 Hard Hats

    Honeywell is recalling specific Fibre-Metal E2 and North Peak A79 hard hats because they may fail to protect users from impact, posing a risk of head injury.

    Product
    Fibre-Metal E2 and North Peak A79 hard hats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V257000·2018-04-20

    Kia Recalls 2017 Niro Vehicles Due to Hybrid System Fire Risk

    Kia is recalling 2017 Niro vehicles because a leaking hydraulic clutch actuator seal may cause an electrical short, increasing the risk of a fire.

    Product
    KIA — KIA NIRO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V255000·2018-04-20

    Altec Recalls 1992-2006 Digger Derrick Trucks Due to Boom Pivot Pin Failure

    Altec Industries is recalling 1992-2006 Digger Derrick trucks because a specific boom pivot pin may fail, causing unexpected boom movement that increases the risk of injury or death.

    Product
    ALTEC — ALTEC DIGGER DERRICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V256000·2018-04-20

    Supreme Recalls 2013-2017 Kold King Vehicles Due to Frame Rail Defect

    Supreme Corporation is recalling 2013-2017 Kold King vehicles because the floor frame rail may detach from cross members due to insufficient weld penetration.

    Product
    SUPREME — SUPREME KOLD KING
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18145·2018-04-20

    Briggs & Stratton Recalls 3000 PSI Pressure Washer Surface Cleaners

    Briggs & Stratton is recalling 3000 PSI pressure washer surface cleaners because the spray bar can break and detach, posing an injury hazard.

    Product
    3000 PSI pressure washer surface cleaners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E024000·2018-04-19

    Bosch Electric Power Steering System Recall for Corroding Bolts

    Bosch is recalling electric power steering systems where aluminum bolts may corrode and fracture, potentially causing loss of steering assist.

    Product
    STEERING:ELECTRIC POWER ASSIST SYSTEM recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V251000·2018-04-19

    Freightliner M2 Trucks Recalled for Rear Brake Caliper Orientation Issue

    Daimler Trucks is recalling 2016-2019 Freightliner Business Class M2 trucks because rear brake calipers may be mounted incorrectly, reducing braking effectiveness.

    Product
    FREIGHTLINER — FREIGHTLINER BUSINESS CLASS M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V249000·2018-04-19

    Coachmen Spirit Recalled for Missing LP Quick Disconnect on Cooktop

    Forest River is recalling 2018-2019 Coachmen Spirit trailers because the outdoor cooktop may lack a liquid propane quick disconnect, posing carbon monoxide and fire risks.

    Product
    COACHMEN — COACHMEN SPIRIT
    Category
    Vehicle
    Distribution
    Distributed nationwide