The Recall Desk

State

Northern Mariana Islands product recalls

73,584 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 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28151–28175 of 73607

  • HighFDA (Devices)·Z-2640-2020·2020-07-29

    EHOB Expansion Control Overlay Recalled for Potential Blood Contamination

    EHOB, Inc. is recalling 173 Expansion Control Overlays (Item No. 1004EC) because a portion of the lot may have been contaminated with blood.

    Product
    Expansion Control Overlay, Item No. 1004EC - Product Usage: The EHOB WAFFLE Overlay is more than a support surface, assisting in lateral transfers, boosts and turns to protect patients throughout the hospital journey. Through immersion and envelopment, the WAFFLE Overlay is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2677-2020·2020-07-29

    Boston Scientific Recalls IceFORCE 2.1 CX Cryoablation Needles

    Boston Scientific is recalling 39 IceFORCE 2.1 CX Cryoablation Needles because the needle surface deteriorated due to unexpected electrolysis during procedures.

    Product
    Ablation Galil Technology, IceFORCE 2.1 CX Needle Cryoablation Needle, Prescription Only Galil Medicals 2.1 CX Cryoablation Needles are intended for cryoablative destruction of tissue during surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2683-2020·2020-07-29

    Boston Scientific Recalls IceForce 2.1 CX Cryoablation Needles

    Boston Scientific is recalling 656 IceForce 2.1 CX Cryoablation Needles because the needle surface deteriorated due to unexpected electrolysis during procedures.

    Product
    Ablation Galil Technology, IceForce 2.1 CX 90 Cyroablation Needles, Prescription Only Galil Medicals 2.1 CX Cryoablation Needles are intended for cryoablative destruction of tissue during surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2687-2020·2020-07-29

    Sysmex PS-10 Sample Preparation System Recalled for Insufficient Antibody

    Sysmex America, Inc. is recalling eight PS-10 Sample Preparation Systems because they may contain insufficient antibody without triggering an error message or alarm.

    Product
    Sysmex PS-10 Sample Preparation System Catalog number:BQ716341 - Product Usage: is a fully automated, user configurable, open system intended for use to prepare human specimens for subsequent analysis on flow cytometers.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2681-2020·2020-07-29

    Boston Scientific Recalls Prostate Cryoablation Kits Due to Needle Surface Deterioration

    Boston Scientific is recalling 71 IceFORCE 2.1 Prostate Cryoablation Kits because needle surfaces deteriorated due to unexpected electrolysis during procedures.

    Product
    Ablation Galil Technology, Three IceFORCE 2.1 Prostate Cyroablation Kit Visual ICE System, Prescription Only Galil Medicals 2.1 CX Cryoablation Needles are intended for cryoablative destruction of tissue during surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V444000·2020-07-29

    Thor Motor Coach motorhomes recalled for faulty swivel seat wiring harnesses

    Certain 2020-2021 Thor motorhomes with swivel seats have wiring harnesses that may be routed incorrectly, potentially causing side airbags to deploy inadvertently or fail during crashes. Owners should contact Thor or Mercedes-Benz for free inspection and repair.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH GEMINI, COMPASS, redundant SYNERGY, CHATEAU CITATION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2675-2020·2020-07-29

    Boston Scientific Recalls IceFORCE Cryoablation Needles Due to Surface Deterioration

    Boston Scientific is recalling 18,440 IceFORCE 2.1 CX 90 Needle Cryoablation Needles because the needle surface deteriorated due to unexpected electrolysis during procedures.

    Product
    Ablation Galil Technology, IceFORCE 2.1 CX 90 Needle Cryoablation Needle, Prescription Only Galil Medicals 2.1 CX Cryoablation Needles are intended for cryoablative destruction of tissue during surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2688-2020·2020-07-29

    Siemens syngo.via RT Image Suite Software Recall for Geometry Errors

    Siemens is recalling syngo.via RT Image Suite software versions VB30 and VB40 because modified MR image orientations may result in incorrect geometry and radiation treatment plans.

    Product
    syngo.via RT Image Suite with software versions syngo.via VB30 or VB40
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2690-2020·2020-07-29

    Medtronic Accurian RF Ablation Cannula Recalled for Insertion Difficulty

    Medtronic is recalling Accurian RF Ablation Cannulas because the probe catches on a lip inside the hub, causing insertion difficulty.

    Product
    Accurian RF Ablation, Cannula pk, Accurian, 100mm, 18G, 10mm, CS Product Number: AC0005 GTIN /UPN: 20763000153551 - Product Usage: (sterile, single-use) comprises an electrically insulated shaft, an active electrode for RF energy delivery, a hub with a female slip luer fitting…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2692-2020·2020-07-29

    Medtronic Accurian RF Ablation Cannula Recall for Insertion Difficulty

    Medtronic is recalling Accurian RF Ablation Cannulas because the probe may catch on a lip inside the hub, causing insertion difficulty.

    Product
    Accurian RF Ablation, Cannula pk, Accurian, 100mm, 20G, 10mm, CS Product Number: AC0009 GTIN / UPN: 20763000153599 - Product Usage: (sterile, single-use) comprises an electrically insulated shaft, an active electrode for RF energy delivery, a hub with a female slip luer fitting…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2691-2020·2020-07-29

    Medtronic Recalls Accurian RF Ablation Cannulas Due to Insertion Difficulty

    Medtronic is recalling Accurian RF Ablation Cannulas because the probes may catch on a lip inside the hub, causing insertion difficulty.

    Product
    Accurian RF Ablation, Cannula pk, Accurian, 150mm, 18G, 10mm, CS Product Number: AC0007 GTIN / UPN: 20763000153568 - Product Usage: (sterile, single-use) comprises an electrically insulated shaft, an active electrode for RF energy delivery, a hub with a female slip luer fitting…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2693-2020·2020-07-29

    Medtronic Accurian RF Ablation Cannula Recalled for Insertion Difficulty

    Medtronic is recalling Accurian RF Ablation Cannulas because the probes catch on a lip inside the hub, causing insertion difficulty.

    Product
    Accurian RF Ablation, Cannula pk, Accurian, 150mm, 20G, 10mm, CS Product Number: AC0012 GTIN / UPN: 20763000153629 - Product Usage: (sterile, single-use) comprises an electrically insulated shaft, an active electrode for RF energy delivery, a hub with a female slip luer fitting…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2695-2020·2020-07-29

    Medtronic Accurian RF Ablation Cannula Recalled for Insertion Difficulty

    Medtronic is recalling Accurian RF Ablation Cannulas because the probe catches on a lip inside the hub, causing insertion difficulty.

    Product
    Accurian RF Ablation,Cannula pk, Accurian, 100mm, 22G, 10mm, SS Product Number: AC0019 GTIN / UPN: 20763000153667 - Product Usage: (sterile, single-use) comprises an electrically insulated shaft, an active electrode for RF energy delivery, a hub with a female slip luer…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2694-2020·2020-07-29

    Medtronic Accurian RF Ablation Cannula Recalled for Insertion Difficulty

    Medtronic is recalling Accurian RF Ablation Cannulas because the probe catches on a lip inside the hub, causing insertion difficulty.

    Product
    Accurian RF Ablation, Cannula pk, Accurian, 100mm, 22G, 5mm, CS Product Number: AC0016 GTIN / UPN: 20763000153674 - Product Usage: (sterile, single-use) comprises an electrically insulated shaft, an active electrode for RF energy delivery, a hub with a female slip luer fitting…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2684-2020·2020-07-29

    Nuvasive NVM5 EMG Module Recalled for Incorrect Component

    NuVasive Inc is recalling 23 NVM5 EMG Modules because they contain an incorrect SSEP harness instead of the correct NVM5 Harness, potentially delaying spinal surgery monitoring.

    Product
    Nuvasive NVM5 EMG Module, REF 8020015, Rx ONLY, CE2797, Nonsterile, UDI: 00887517206633 - Product Usage: is intended for intraoperative neurophysiologic monitoring during spinal surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalCPSC·20157·2020-07-28

    Triangle Tube Recalls Prestige Gas Boilers Due to Carbon Monoxide Risk

    Triangle Tube is recalling about 63,000 Prestige Solo and Excellence gas boilers because a vent adapter may detach, causing carbon monoxide leaks. One death was reported.

    Product
    Prestige Solo & Prestige Excellence condensing gas boilers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V432000·2020-07-28

    High Altitude Trailer XT50 Recalled for Rear Swing Arm Weld Failure

    High Altitude Trailer is recalling 2019-2020 XT50 trailers with retrofitted rear swing arm spare tire carriers because a weld may fail, causing the tire to separate and increasing crash risk.

    Product
    HIGH ALTITUDE TRAILER — HIGH ALTITUDE TRAILER XT50
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E051000·2020-07-28

    Meritor Recalls P220 and P579 Pressure Assemblies Due to Hose Fitting Defect

    Meritor is recalling specific pressure assemblies where an incorrect fitting may cause the power steering hydraulic hose to fail, resulting in a loss of steering assist.

    Product
    STEERING:HYDRAULIC POWER ASSIST:HOSE, PIPING, AND CONNECTIONS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V435000·2020-07-28

    Daimler Recalls 2021 Thomas Built Buses Saf-T-Liner C2 School Buses

    Daimler Trucks North America is recalling 2021 Saf-T-Liner C2 School Buses because the brake pedal arm may rotate out of position, increasing crash risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V434000·2020-07-28

    BMW Recalls 2019-2020 X5 and X6 M for Steering Column Defect

    BMW is recalling 2019-2020 X5 and 2020 X6 M vehicles because the steering column shaft bearing plate may not be properly attached, which can affect handling and increase crash risk.

    Product
    BMW — BMW X5, X6 M
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V438000·2020-07-28

    Honda Recalls 2019-2020 Odyssey Vehicles for Rearview Camera Defect

    Honda is recalling 2019-2020 Odyssey vehicles because water intrusion can cause the rearview camera to display a distorted or no image, increasing crash risk.

    Product
    HONDA — HONDA ODYSSEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V439000·2020-07-28

    Honda Odyssey, Passport, and Pilot instrument panel and rearview camera software failure

    Honda is recalling 2018-2020 Odyssey, 2019-2020 Passport, and 2019-2021 Pilot vehicles with software causing the instrument panel to fail to display critical information (engine oil pressure, speedometer, gear position) and preventing the rearview camera image from displaying.

    Product
    HONDA — HONDA PILOT, ODYSSEY, PASSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V433000·2020-07-28

    Tiffin Recalls Motorhomes Due to Windshield Wiper Wiring Defect

    Tiffin is recalling 2018-2020 Zephyr and 2019-2020 Bus motorhomes because improperly wired control modules may cause windshield wipers to stop working.

    Product
    TIFFIN — TIFFIN ZEPHYR, BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide