The Recall Desk

State

Northern Mariana Islands product recalls

73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

33001–33025 of 73745

  • HighNHTSA·19V530000·2019-07-14

    BYD Recalls 2019 C8M Buses Due to Glass Roof Hatch Shattering Risk

    BYD is recalling 2019 C8M buses because temperature and vibration stresses may cause the tempered glass roof escape hatches to shatter, potentially injuring passengers.

    Product
    BYD — BYD C8M
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V526000·2019-07-12

    Blue Bird Recalls School Buses Due to Roof Hatch Handle Defect

    Blue Bird is recalling 2018-2020 Vision and All American school buses because the roof emergency exit handle may break, preventing easy opening during an emergency.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN, VISION, VISION SCHOOL BUS, ALL AMERICAN SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V523000·2019-07-12

    Spartan Gladiator and MetroStar Front Shock Separation Recall

    Spartan is recalling 2014-2020 Gladiator and MetroStar vehicles because front shocks may separate, potentially causing a loss of power steering assist and increasing crash risk.

    Product
    SPARTAN — SPARTAN GLADIATOR, METROSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V529000·2019-07-12

    American Coach Motorhomes Recalled for Rear Air Deflector Detachment Risk

    REV Recreation Group is recalling 2016-2019 American Coach motorhomes because rear air deflectors may detach, creating a road hazard.

    Product
    AMERICAN COACH — AMERICAN COACH AMERICAN HERITAGE, AMERICAN EAGLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V525000·2019-07-12

    Heartland Recalls Fifth-Wheel Trailers Due to A/C Electrical Connector Fire Risk

    Heartland is recalling specific 2016-2020 fifth-wheel trailers because an improperly installed A/C electrical connector may overheat and increase the risk of a fire.

    Product
    HEARTLAND — HEARTLAND PIONEER, NORTH PEAK, MILESTONE, ELKRIDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V524000·2019-07-12

    Blue Bird Recalls 2020 School Buses for Roof Hatch Handle Defect

    Blue Bird is recalling 2020 Vision and All American school buses because the roof hatch handle may break, preventing emergency exit.

    Product
    BLUE BIRD — BLUE BIRD VISION SCHOOL BUS, ALL AMERICAN SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V528000·2019-07-12

    KME Fire Trucks Recalled for Cab Hydraulic Velocity Fuse Defect

    KME is recalling various 2016-2020 Predator and Predator Panther fire trucks because hydraulic velocity fuses may fail to lock the cab during a system failure, posing an injury risk to occupants.

    Product
    KME — KME PREDATOR PANTHER PUMPER, PREDATOR SS PUMPER, PREDATOR SS RESCUE, PREDATOR AERIAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19164·2019-07-11

    Lidl Recalls Wooden Grasping Toys Due to Choking Hazard

    Lidl is recalling Playtive Junior Wooden Grasping Toys because the wheels can detach, posing a choking hazard to young children.

    Product
    Playtive Junior Wooden Grasping Toy
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19761·2019-07-11

    Levolor Recalls Custom Cellular Shades Due to Strangulation Hazard

    Levolor is recalling about 30,000 custom cellular shades because the pull cords are joined by a non-breakaway connector, posing a strangulation hazard to small children.

    Product
    Levolor Two-Corded Custom Cellular Shades
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19165·2019-07-11

    Lifetime Brands Recalls Fitz and Floyd Can Mugs Due to Burn Hazards

    Lifetime Brands is recalling Fitz and Floyd Nevaeh White can mugs because they can crack or break when exposed to hot liquids, posing burn and laceration hazards.

    Product
    Fitz and Floyd® Nevaeh White® Can Mugs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V520000·2019-07-11

    Micro Bird Recalls 2019 MB II Buses Due to Fire Risk

    Micro Bird is recalling 52 model-year 2019 MB II propane-powered buses because a melted grounding wire could cause an engine compartment fire.

    Product
    MICRO BIRD — MICRO BIRD MB II TRANSIT BUS, MB II SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1488-2019·2019-07-10

    PharMEDium Recalls Hydromorphone Syringes Due to Sulfite Mislabeling

    PharMEDium Services is recalling 28,140 hydromorphone syringes because the product is labeled as sulfite-free but contains sulfites.

    Product
    Hydromorphone HCl in 0.9% sodium chloride, 0.5mg per mL, 1 mL in 3mL BD Syringe, PharMEDium 913 N Davis Ave Cleveland, MS 38732, 800-523-7749, NDC 61553-352-78
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1905-2019·2019-07-10

    Siemens Fluoroscopic X-Ray Systems Recalled for Potential Screw Failure

    Siemens is recalling eight Artis fluoroscopic X-ray systems because screws on the ceiling-mounted support may loosen or snap, posing a risk of severe injury.

    Product
    Siemens Artis pheno-Interventional Fluoroscopic X-Ray System Model Number: 10849000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1894-2019·2019-07-10

    Siemens Artis zee X-Ray Systems Recalled for Ceiling Support Screw Failure

    Siemens is recalling 63 Artis zee X-ray systems because ceiling support screws may loosen or snap, posing a risk of severe injury to patients and staff.

    Product
    Siemens Artis zee floor -Interventional Fluoroscopic X-Ray System Model Number: 10094135
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1897-2019·2019-07-10

    Siemens Artis X-Ray Systems Recalled for Ceiling Mount Screw Failure Risk

    Siemens is recalling 29 Artis X-ray systems because ceiling mount screws may loosen or snap, posing a risk of severe injury to patients and staff.

    Product
    Siemens Artis zeego--Interventional Fluoroscopic X-Ray System Model Number: 10280959
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V517000·2019-07-10

    Keystone Recalls 2020 Crossroads Trailers Due to Brake Wiring Defect

    Keystone is recalling 2020 Crossroads Hampton and Sunset trailers because an incorrectly wired breakaway switch may prevent brakes from functioning if the trailer separates from the tow vehicle.

    Product
    CROSSROADS — CROSSROADS HAMPTON, SUNSET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1896-2019·2019-07-10

    Siemens Artis X-Ray Systems Recalled for Ceiling Mount Screw Failure

    Siemens is recalling 120 Artis X-Ray systems because ceiling-mounted support screws may loosen or snap, posing a risk of severe injury to patients and staff.

    Product
    Siemens Artis zee biplane-Interventional Fluoroscopic X-Ray System Model Number: 10094141
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1898-2019·2019-07-10

    Siemens Artis X-Ray Systems Recalled for Ceiling Support Screw Failure

    Siemens is recalling 12 Artis X-ray systems because ceiling-mounted support screws may loosen or snap, posing a risk of severe injury to patients and staff.

    Product
    Siemens Artis Q floor --Interventional Fluoroscopic X-Ray System Model Number: 10848280
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1904-2019·2019-07-10

    Siemens Artis X-Ray Systems Recalled for Ceiling Mount Screw Failure Risk

    Siemens is recalling 11 Artis X-ray systems because ceiling-mounted support screws may loosen or snap, posing a risk of severe injury to patients and staff.

    Product
    Siemens Artis Q.zen biplane-Interventional Fluoroscopic X-Ray System Model Number: 10848355
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1895-2019·2019-07-10

    Siemens Artis zee Ceiling X-Ray System Recall for Loose Screws

    Siemens is recalling 276 Artis zee ceiling-mounted X-ray systems because screws joining the pivot bearing to the ceiling support may work loose or snap off, posing a risk of severe injury.

    Product
    Siemens Artis zee ceiling -Interventional Fluoroscopic X-Ray System Model Number: 10094137
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1901-2019·2019-07-10

    Siemens Artis X-Ray Systems Recalled Due to Ceiling Mount Screw Failure Risk

    Siemens is recalling two Artis Q zeego X-ray systems because ceiling-mounted support screws may loosen or snap, posing a risk of severe injury to patients and staff.

    Product
    Siemens Artis Q zeego ---Interventional Fluoroscopic X-Ray System Model Number: 10848283
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1899-2019·2019-07-10

    Siemens Artis X-Ray Systems Recalled for Ceiling Mount Screw Failure Risk

    Siemens is recalling 131 Artis X-ray systems because ceiling mount screws may loosen or snap, posing a risk of severe injury to patients and staff.

    Product
    Siemens Artis Q ceiling--Interventional Fluoroscopic X-Ray System Model Number: 10848281
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1902-2019·2019-07-10

    Siemens Artis X-Ray Systems Recalled for Potential Screw Failure

    Siemens is recalling eight Artis X-ray systems because screws on the ceiling-mounted support may loosen or snap, posing a risk of severe injury to patients and staff.

    Product
    Siemens Artis Q.zen floor----Interventional Fluoroscopic X-Ray System Model Number: 10848353
    Category
    Medical Device
    Distribution
    Distributed nationwide