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.

58076–58100 of 73856

  • ModerateFDA (Devices)·Z-1778-2014·2014-06-18

    Stryker Precision Neuro Drill Recall Due to Missing Notches

    Stryker is recalling 6,481 Precision Neuro Drills because some cutting accessories may have missing or partial notches, which could affect their use with Elite Attachments.

    Product
    Stryker 3.0mm x 3.8mm Precision Neuro Drill Sterile Product Usage: The devices are intended to be used to cut bone and bone related tissue during neurosurgery, including craniotomy and spinal surgery as well as ear, nose and throat (ENT), orthopedic, and general surgical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1761-2014·2014-06-18

    Stryker Elite Bur Recall Due to Missing Notches

    Stryker is recalling 2.0mm Tapered Round Elite Burs because some units have missing or partial notches. The devices are used for cutting bone during surgery.

    Product
    Stryker 2.0mm Tapered Round Elite Bur Sterile Product Usage: The devices are intended to be used to cut bone and bone related tissue during neurosurgery, including craniotomy and spinal surgery as well as ear, nose and throat (ENT), orthopedic, and general surgical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1738-2014·2014-06-18

    Ortho-Clinical enGen Laboratory Automation Systems Recalled for Software Anomaly

    Ortho-Clinical Diagnostics is recalling enGen Laboratory Automation Systems with specific TCAutomation software versions due to a potential delay in reporting patient sample test results.

    Product
    enGen Laboratory Automation Systems (enGen) with TCAutomation -- For in vitro quantitative measurement of a variety of analytes of clinical interest; for pre-analytical and post-analytical sample and data management. --- Background: The enGen Lab Automation System is a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1749-2014·2014-06-18

    Stryker 0.5mm Round Fluted Bur Recalled for Missing Notches

    Stryker is recalling 27 sterile 0.5mm Round Fluted Burs because some units may have missing or partial notches, which could affect their use with Elite Attachments.

    Product
    Stryker 0.5mm Round Fluted Bur Sterile Product Usage: The devices are intended to be used to cut bone and bone related tissue during neurosurgery, including craniotomy and spinal surgery as well as ear, nose and throat (ENT), orthopedic, and general surgical applications…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1779-2014·2014-06-18

    Stryker 5.0mm Barrel Bur Recall for Missing Notches

    Stryker is recalling 5.0mm Barrel Bur devices because some units have missing or partial notches, which may affect their use with Elite Attachments.

    Product
    Stryker 5.0mm Barrel Bur Sterile Product Usage: The devices are intended to be used to cut bone and bone related tissue during neurosurgery, including craniotomy and spinal surgery as well as ear, nose and throat (ENT), orthopedic, and general surgical applications…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1737-2014·2014-06-18

    Beckman Coulter Recalls Ultrasonic Transducer Kits Due to Incorrect Screws

    Beckman Coulter is recalling 82 Ultrasonic Transducer Kits because they may have been assembled with incorrect mounting screws.

    Product
    Ultrasonic Transducer Kits For use with the Access Family of Immunoassay Systems*. *The Access Family of Immunoassay Systems includes the Access 2, UniCel DxI 800 and UniCel DxI 600, UniCel DxC 600i, and the UniCel DxC 880i, UniCel DxC 860i, UniCel DxC 680i, and UniCel DxC…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1780-2014·2014-06-18

    Stryker Neuro Drill Accessories Recalled for Missing Notches

    Stryker is recalling 916 sterile neuro drill cutting accessories due to missing or partial notches that may affect device performance.

    Product
    Stryker 3.0mm x 3.8mm Neuro Drill Less Aggressive Sterile Product Usage: The devices are intended to be used to cut bone and bone related tissue during neurosurgery, including craniotomy and spinal surgery as well as ear, nose and throat (ENT), orthopedic, and general…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1757-2014·2014-06-18

    Stryker 4.5mm Round Fluted Bur Recall for Missing Notches

    Stryker is recalling 62 units of 4.5mm Round Fluted Bur Aggressive Sterile devices due to missing or partial notches.

    Product
    Stryker 4.5mm Round Fluted Bur Aggressive Sterile Product Usage: The devices are intended to be used to cut bone and bone related tissue during neurosurgery, including craniotomy and spinal surgery as well as ear, nose and throat (ENT), orthopedic, and general surgical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1763-2014·2014-06-18

    Stryker Recalls Four Zyphr Elite Round Fluted Bur Units

    Stryker is recalling four sterile Zyphr Elite Round Fluted Bur units due to missing or partial notches that may affect compatibility with Elite attachments.

    Product
    Stryker 5.0mm Zyphr Elite Round Fluted Bur Sterile Product Usage: The devices are intended to be used to cut bone and bone related tissue during neurosurgery, including craniotomy and spinal surgery as well as ear, nose and throat (ENT), orthopedic, and general surgical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1773-2014·2014-06-18

    Stryker Wire Pass Drill Recalled for Missing Notches

    Stryker is recalling 246 sterile 1.5mm Wire Pass Drills because some units may have missing or partial notches, which could affect their use with Elite Attachments.

    Product
    Stryker 1.5mm Wire Pass Drill Sterile Product Usage: The devices are intended to be used to cut bone and bone related tissue during neurosurgery, including craniotomy and spinal surgery as well as ear, nose and throat (ENT), orthopedic, and general surgical applications…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1766-2014·2014-06-18

    Stryker 5.0mm Egg Bur Recall Due to Missing Notches

    Stryker is recalling 144 units of 5.0mm Egg Bur sterile devices because some cutting accessories may have missing or partial notches.

    Product
    Stryker 5.0mm Egg Bur Sterile Product Usage: The devices are intended to be used to cut bone and bone related tissue during neurosurgery, including craniotomy and spinal surgery as well as ear, nose and throat (ENT), orthopedic, and general surgical applications including…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·14V331000·2014-06-17

    American Coach Recalls 2015 Motor Homes Due to Seat Belt Defect

    Allied Recreation Group is recalling 2015 American Coach motor homes because incorrect seat belt installation may cause fraying and reduced strength.

    Product
    AMERICAN COACH — AMERICAN COACH AMERICAN EAGLE, AMERICAN TRADITION, AMERICAN REVOLUTION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V333000·2014-06-17

    Lion 360 School Bus Seat Belt Buckle Recall

    Lion Bus is recalling 2014 360 school buses because seat belt buckles may fail to release, hindering emergency egress.

    Product
    LION — LION 360
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V330000·2014-06-17

    American Coach Motor Homes Recalled for Defective Seat Belt Attachments

    Allied Recreation Group is recalling 2013-2014 American Coach motor homes because incorrect seat belt attachments may cause fraying and reduced strength.

    Product
    AMERICAN COACH — AMERICAN COACH AMERICAN EAGLE, AMERICAN REVOLUTION, AMERICAN TRADITION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V329000·2014-06-16

    MCI Motor Coaches Recalled for Interior Lighting Fire Risk

    Motor Coach Industries is recalling certain 2009-2011 MCI D4000, D4500, and 2010 D4505 motor coaches because excessive power draw from LED interior lights may cause heat buildup and fire.

    Product
    MCI — MCI D4000, D4500, D4505
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V323000·2014-06-13

    Honda Recalls Acura ILX Vehicles for Headlight Fire Risk

    Honda is recalling certain 2013-2014 Acura ILX vehicles because excessive heat around the headlight bulb may cause smoke, melting, or fire, increasing crash risk.

    Product
    ACURA — ACURA ILX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V328000·2014-06-13

    Ford F-Series Trucks Recalled for PTO Switch Fire Risk

    Iowa Mold Tooling is recalling 2009-2014 Ford F-350, F-450, and F-550 SD trucks because a leaking PTO pressure switch may cause a fire.

    Product
    FORD — FORD F-450 SD, F-350 SD, F-550 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14E030000·2014-06-13

    Meritor Recalls MFS12143ANN Axles Due to Weak Beam Spots

    Meritor is recalling specific MFS12143ANN non-drive steer axles because manufacturing errors may have created weak spots in the beam, increasing the risk of sudden axle failure and a crash.

    Product
    SUSPENSION:FRONT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V326000·2014-06-13

    Manning Recalls Modified Ford Super Duty Trucks Due to Fire Risk

    Manning Equipment is recalling 2012-2013 modified Ford Super Duty trucks because oil leaks from the PTO pressure switch onto the exhaust thermal blanket, increasing fire risk.

    Product
    FORD — FORD F-350 SD, F-450 SD, F-550 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V320000·2014-06-12

    BMW Recalls 2014 R 1200 RT Motorcycles for Rear Shock Absorber Defect

    BMW is recalling 950 model year 2014 R 1200 RT motorcycles because the rear shock absorber piston rod can break, causing loss of stability and increasing crash risk.

    Product
    BMW — BMW R 1200 RT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V322000·2014-06-12

    Winnebago Recalls 2014-2015 Motorhomes for Electrical Corrosion Risk

    Winnebago is recalling 2014-2015 Travato, Trend, and Itasca Viva motorhomes because water intrusion may cause electrical corrosion that disables safety features.

    Product
    WINNEBAGO — WINNEBAGO TRAVATO, ITASCA VIVA, TREND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V319000·2014-06-12

    Harley-Davidson Recalls 2014 Touring Motorcycles Due to Brake Line Pinch Risk

    Harley-Davidson is recalling 66,421 model year 2014 Touring and CVO Touring motorcycles because a front brake line may be pinched, potentially causing front wheel lock-up and increasing crash risk.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON FLHR, FLHXSHRINE, FLHXS, FLHTCU
    Category
    Vehicle
    Distribution
    Distributed nationwide