The Recall Desk

State

Northern Mariana Islands product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

51351–51375 of 73840

  • ModerateFDA (Devices)·Z-0192-2016·2015-11-04

    Synthes Threaded Plate Holder Recalled for Incorrect Part Number Etching

    Synthes (USA) Products LLC is recalling 25 units of Threaded Plate Holders that are incorrectly etched with the wrong part number and may not fit into a Small Fragment Plate.

    Product
    Synthes Threaded Plate Holder- Long for 3.5mm Locking Hold; Part Numbers 324.031. The Threaded Plate Holder can be used as an aid to position the plate on the bone. The plate holder may also function as an insertion handle for use with minimally invasive plating techniques.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0176-2016·2015-11-04

    Philips Ingenuity Core 128 CT Systems Recalled for X-ray Measurement Error

    Philips Medical Systems is recalling 109 Ingenuity Core 128 CT systems due to X-ray measurement errors causing image artifacts.

    Product
    Ingenuity Core 128 Computed Tomography X-ray systems. Intended to produce cross-sectional images of the body.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0164-2016·2015-11-04

    Sentinel Ammonia Reagent Recalled for Inaccurate Results in Heparin Tubes

    Sentinel CH SpA is recalling 765 kits of Sentinel MULTIGENT Ammonia Ultra Reagent because results may be below the linear range for samples collected in heparin tubes.

    Product
    Sentinel MULTIGENT Ammonia Ultra Reagent, In-Vitro Diagnostic for ammonia measurement; List Number: LN 6K89-30. Intended for the in vitro quantitative determination of Ammonia (NH3) in human plasma.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0174-2016·2015-11-04

    Philips Recalls Brilliance 64 CT Systems Due to X-ray Measurement Error

    Philips Medical Systems is recalling 108 Brilliance 64 CT systems worldwide due to an X-ray measurement error that causes Ring/Dot artifacts.

    Product
    Brilliance 64 Computed Tomography X-ray systems. Intended to produce cross-sectional images of the body.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0175-2016·2015-11-04

    Philips Ingenuity Core CT Systems Recalled for X-ray Measurement Error

    Philips is recalling 36 Ingenuity Core CT systems worldwide due to an X-ray measurement error that causes Ring/Dot artifacts in images.

    Product
    Ingenuity Core Computed Tomography X-ray systems. Intended to produce cross-sectional images of the body.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0173-2016·2015-11-04

    Philips Recalls Brilliance 16-Slice CT Systems Due to X-ray Measurement Error

    Philips Medical Systems is recalling 323 Brilliance 16-Slice CT systems worldwide due to X-ray measurement errors causing Ring/Dot artifacts.

    Product
    Brilliance 16-Slice (Air) Computed Tomography X-ray systems. Intended to produce cross-sectional images of the body.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0170-2016·2015-11-04

    Varian ARIA Radiation Oncology Software Recall for Printing Anomaly

    Varian Medical Systems is recalling ARIA Radiation Oncology software versions 10, 11, 13.0, and 13.5 because admin instructions may fail to print or transmit.

    Product
    ARIA Radiation Oncology, versions 10, 11 , 13.0 and 13.5 with Clinical Assessment License. Model number HIT Product Usage: ARIA Radiation Oncology is a radiation treatment plan and image management application.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0178-2016·2015-11-04

    Philips Recalls Ingenuity Flex CT Systems Due to X-ray Measurement Error

    Philips Medical Systems is recalling 67 Ingenuity Flex CT systems worldwide due to an X-ray measurement error that causes Ring/Dot artifacts in images.

    Product
    Ingenuity Flex Computed Tomography X-ray systems. Intended to produce cross-sectional images of the body.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0171-2016·2015-11-04

    BD CD3 FITC Recalled for Spanish Labeling Error

    Becton, Dickinson and Company is recalling two lots of BD CD3 (SK7) FITC in vitro diagnostic reagents due to an error in the Spanish small text on the label.

    Product
    BD CD3 (SK7) FITC; IVD; Catalog # 349201 and 340542 Hematology: The CD3 antibody reacts with the epsilon chain of the CD3 antigen/T-cell antigen receptor (TCR) complex. In vitro diagnostic.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V725000·2015-11-03

    Prevost Recalls 2016 Coaches Due to Front Suspension Stud Failure Risk

    Prevost is recalling 2016 H3-45 and X3-45 VIP coaches because front suspension studs may fail, allowing a wheel to turn unexpectedly and increasing crash risk.

    Product
    PREVOST — PREVOST H3-45 VIP, H3-45, X3-45 VIP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·16025·2015-11-03

    GE Recalls Zoneline Air Conditioners and Heating Units Due to Fire Risk

    GE is recalling about 33,500 Zoneline air conditioning and heating units due to a risk of fire caused by moisture accumulation and electrical arcing.

    Product
    GE Zoneline® Air Conditioners and Heating Units
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V728000·2015-11-03

    Toyota Recalls 2013-2015 Avalon and Lexus ES for Braking Defect

    Toyota is recalling 2013-2015 Avalon and Lexus ES vehicles because the Pre-Collision System may unexpectedly brake when detecting steel road objects.

    Product
    LEXUS — LEXUS, TOYOTA ES HYBRID, ES350, AVALON HYBRID, AVALON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V726000·2015-11-03

    Forest River Recalls 2016 Recreational Vehicles Due to Shift Cable Defect

    Forest River is recalling 217 model year 2016 recreational vehicles because an incorrect shift cable bracket allows the vehicle to be shifted out of park without applying the brakes.

    Product
    FOREST RIVER — FOREST RIVER, COACHMEN FR3, GEORGETOWN, MIRADA, PURSUIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V724000·2015-11-03

    Diamond Coach Recalls 2006-2011 Buses with Defective Wheelchair Lifts

    Diamond Coach is recalling 49 model year 2006-2011 PT and VIP transit buses equipped with certain Ricon wheelchair lifts. The lifts may have oversized pivot holes that allow bearings to move, potentially causing the platform to fall out of the vehicle.

    Product
    DIAMOND COACH — DIAMOND COACH PT, VIP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16705·2015-11-03

    Carra Imports Recalls Window Shades Due to Strangulation Hazard

    Carra Imports is recalling about 55,500 custom window shades due to a strangulation hazard involving continuous loop cords or exposed inner cords.

    Product
    Window shades
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V723000·2015-11-02

    KME Recalls 2016 Predator and Severe Service Vehicles for Axle Defect

    KME is recalling 2016 Predator and Severe Service vehicles because improperly tightened axle hex nuts may cause the driveshaft to disconnect, increasing crash risk.

    Product
    KME — KME SEVERE SERVICE, PREDATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V721000·2015-11-02

    Indian Motorcycle Recalls 2015-2016 Models Due to Rear Brake Failure

    Indian Motorcycle is recalling 7,614 motorcycles from 2015-2016 because a rear brake master cylinder defect may cause a loss of braking power.

    Product
    INDIAN — INDIAN CHIEF CLASSIC, CHIEF VINTAGE, CHIEFTAIN, ROADMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V722000·2015-11-02

    Trans Tech School Buses Recalled for Wheelchair Lift Bearing Defect

    Transportation Collaborative is recalling 188 Trans Tech school buses equipped with certain Ricon wheelchair lifts. Defective pivot holes may allow bearings to shift, causing the lift platform to fall and injure operators.

    Product
    TRANS TECH BUS — TRANS TECH BUS, TRANS TECH STUDENT SAFETY TRANSPORT, ROADSTER, ST AERO, ROADSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V720000·2015-11-02

    McNeilus Front Loader Trucks Recalled for Hydraulic Fire Risk

    McNeilus is recalling 2012-2015 front loader trucks because a hydraulic test port tube may crack, allowing fluid to contact hot exhaust components and increase fire risk.

    Product
    MCNEILUS — MCNEILUS ATLANTIC FRONT LOADER, PACIFIC FRONT LOADER, CONTENDER FRONT LOADER, ULTRA FRONT LOADER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·135-2015·2015-11-01

    All American Meats Recalls Ground Beef Due to E. Coli O157:H7 Risk

    All American Meats is recalling approximately 167,427 pounds of ground beef products due to possible E. coli O157:H7 contamination. No illnesses have been reported.

    Product
    All American Meats, Inc. — All American Meats, Inc. Recalls Ground Beef Products Due to Possible E. Coli O157:H7 Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V717000·2015-10-30

    Porsche Recalls 2015-2016 Macan S and Turbo for Fuel Line Leak

    Porsche is recalling 21,835 Macan S and Turbo vehicles because a low-pressure fuel line may leak, increasing the risk of fire.

    Product
    PORSCHE — PORSCHE MACAN S, MACAN TURBO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V544000·2015-10-30

    GM Recalls 2013-2014 CNG Vehicles for Small Fuel Label

    General Motors is recalling 2013-2014 Chevrolet and GMC CNG vehicles because the fuel-only label is smaller than required, which may increase fire risk.

    Product
    CHEVROLET — CHEVROLET, GMC EXPRESS, SILVERADO, SAVANA, SIERRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V719000·2015-10-30

    Thor Motor Coach Recalls 2016 RVs for Transmission Shift Cable Defect

    Thor Motor Coach is recalling 2016 Ace, Challenger, Hurricane, Miramar, Outlaw, and Windsport vehicles because they may shift out of park without brakes applied.

    Product
    THOR MOTOR — THOR MOTOR, THOR MOTOR COACH HURRICANE, OUTLAW, MIRAMAR, WINDSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V718000·2015-10-30

    BMW Recalls 2016 Models for Bent Child Seat Anchor Defect

    BMW is recalling 2016 5 Series and M5 sedans because a bent child seat anchor may prevent proper engagement, increasing injury risk in a crash.

    Product
    BMW — BMW 528I, 535D, 535I, M5
    Category
    Vehicle
    Distribution
    Distributed nationwide