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.

41201–41225 of 73764

  • SevereNHTSA·17E048000·2017-08-28

    Ford Recalls Wheel Hub Bearings for 2011-2017 Explorer 4X2 Vehicles

    Ford is recalling certain wheel hub bearing assemblies for 2011-2017 Ford Explorer 4X2 vehicles because they lack a self-retention feature, which could cause the wheel to separate.

    Product
    FORD — FORD EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V531000·2017-08-28

    Triton Recalls 2017 W-25 Trailers Due to Axle Bolt Tightening Defect

    Triton Trailers is recalling 2017 W-25 Single Torsion Axle Trailers because improperly tightened axle mounting bolts may cause the axle to detach, increasing crash risk.

    Product
    TRITON — TRITON W-25
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V529000·2017-08-28

    Ford Recalls 2017 F-150 and Mustang for Air Bag Inflator Defect

    Ford is recalling 2017 F-150 and Mustang vehicles because the passenger air bag inflator may rupture in a crash, potentially causing serious injury or death.

    Product
    FORD — FORD F-150, MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V528000·2017-08-28

    Ford Recalls 2017 Focus Vehicles for Rear Seat Back Weld Defect

    Ford is recalling 2017 Focus vehicles because an insufficient weld on the rear left seat back may reduce its strength, increasing injury risk in a crash.

    Product
    FORD — FORD FOCUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V530000·2017-08-28

    Ford Recalls 2017 Models for Steering Gear Heat Shield Fastener Defect

    Ford is recalling 2017 Explorer, Taurus, and Police Interceptor vehicles because steering gear heat shield fasteners may corrode and detach, potentially causing overheating and increased steering effort.

    Product
    FORD — FORD EXPLORER, TAURUS, POLICE INTERCEPTOR SEDAN, POLICE INTERCEPTOR UTILIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V532000·2017-08-28

    Hyundai Recalls 2017 Ioniq Electric Vehicles for Electronic Power Control Unit Defect

    Hyundai is recalling 2017 Ioniq Electric vehicles because a manufacturing defect in the Electronic Power Control Unit may allow coolant to contact the circuit board, potentially causing a stall and increasing crash risk.

    Product
    HYUNDAI — HYUNDAI IONIQ ELECTRIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V526000·2017-08-28

    Ford Recalls F-150 and F-250 Trucks for Seat Belt Defect

    Ford is recalling 2015-2017 F-150 and 2017 F-250/F-350 trucks because the left rear inflatable seat belt buckle may detach, increasing injury risk.

    Product
    FORD — FORD F-150, F-250 SD, F-350 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V523000·2017-08-25

    Forest River Recalls 2018 XLR ToyHaulers for Incorrect Tire Placard Information

    Forest River is recalling 2018 XLR ToyHaulers because the Federal Placard may display incorrect tire and rim specifications, potentially leading to the installation of incorrect replacement tires.

    Product
    FOREST RIVER — FOREST RIVER XLR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V521000·2017-08-24

    Western Star 4900 Trucks Recalled for Front Axle Spring Defect

    Daimler Trucks North America is recalling 2017-2018 Western Star 4900 trucks because front axle weight capacity may exceed spring capacity, risking axle separation.

    Product
    WESTERN STAR — WESTERN STAR 4900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V522000·2017-08-24

    Thor Motor Coach Recalls 2018 RVs for Propane Hose Leak Risk

    Thor Motor Coach is recalling 2018 Four Winds, Chateau, and Freedom Elite recreational vehicles because a liquid propane hose may sag and pinch, potentially causing a leak and fire risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH FREEDOM ELITE, CHATEAU, FOUR WINDS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17211·2017-08-24

    Dr. Martens Vegan Boots Recalled for Benzidine Chemical Exposure Hazard

    Airwair is recalling Dr. Martens Vegan 1460 boots in cherry red because the tongue lining contains benzidine. Consumers should stop using the boots and contact Dr. Martens for a refund or replacement.

    Product
    Dr. Martens Vegan boots
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1092-2017·2017-08-23

    GEC LX Laxoplex Recalled for Undeclared Anabolic Steroids

    Genetic Edge Compounds LLC is recalling GEC LX Laxoplex dietary supplements because FDA analysis found the product tainted with undeclared anabolic steroids and steroid-like substances.

    Product
    GEC LX Laxoplex 60 capsules Dietary Supplement, 60 count bottle, Manufactured by GEC, McKinney, TX, 75070, UPC: 700580499842
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1087-2017·2017-08-23

    Biotech Underground Tri-Ton Hardcore Formula Recalled for Unapproved Ingredients

    Dynamic Technical Formulations is recalling Biotech Underground Tri-Ton Hardcore Formula capsules because FDA testing found unapproved drug ingredients.

    Product
    Biotech Underground Tri-Ton Hardcore Formula capsules, 90-count bottle, Distributed by: Dynamic Technical Formulations 12850 Hwy 9 Suite 600-441 Alpharetta, GA 30004
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3367-2017·2017-08-23

    NatureAll Acidophilus-Plus Recalled for Undeclared Milk Allergens

    NatureAll is recalling Acidophilus-Plus dietary supplements because they contain undeclared milk allergens, including colostrum, dried yogurt, and whey.

    Product
    Acidophilus-Plus, No. 102, 90 Capsules, Dietary Supplement,
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3038-2017·2017-08-23

    Boston Scientific Recalls Emblem MRI S-ICD Devices Due to Energy Delivery Risk

    Boston Scientific is recalling approximately 9,200 Emblem MRI S-ICD devices because memory corruption may cause the device to deliver an atypical amount of energy.

    Product
    EMBLEM MRI S-ICD Model 219, Subcutaneous-Implantable Cardioverter Defibrillator, Rx. Product Usage: The S-ICD system is intended to provide defibrillation therapy for the treatment of life-threatening ventricular tachyarrhythmias in patients who do not have symptomatic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1085-2017·2017-08-23

    Hardcore Formulations Recalls D-ZINE Rapid Size and Strength Capsules

    Hardcore Formulations is recalling D-ZINE Rapid Size and Strength capsules because they contain unapproved active ingredients.

    Product
    D-ZINE Rapid Size and Strength capsules, 10mgs, 90 count bottle, Hardcore Formulations, UPC: 7 48252 86193 1
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3034-2017·2017-08-23

    Cenorin ThermaSure Medical Device Dryers Recalled for Overheating Terminal Block

    Cenorin, LLC is recalling 18 ThermaSure Series 1000 medical device dryers because a manufacturing defect causes the terminal block to overheat, char, or burn.

    Product
    ThermaSure(TM), a CENORIN(TM) product, SERIES 1000 MEDICAL DEVICE DRYER: (a) Model 1009; (b) Model 1010 Forced air dryer for medical devices
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1084-2017·2017-08-23

    FDA Recalls Ultra-Sten Capsules Marketed Without Approval

    Hardcore Formulations is recalling Ultra-Sten capsules because they contain unapproved ingredients and were marketed without an approved NDA or ANDA.

    Product
    ULTRA-STEN Rapid Size and Strength capsules, 10 mgs, 90 count bottle, Hardcore Formulations UPC: 7 48252 68763 0
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1091-2017·2017-08-23

    ICU Medical Recalls 0.9% Sodium Chloride Injection Due to Particulate Matter

    ICU Medical Inc. is recalling 436,716 units of 0.9% Sodium Chloride Injection due to the presence of stainless steel particulate matter.

    Product
    0.9% Sodium Chloride Injection, USP in 1000 mL Single Dose Flexible Container, Hospira, Inc., Lake Forest, IL 60045 USA --- NDC# 0409-7983-09
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3039-2017·2017-08-23

    Boston Scientific Recalls SQ-RX 1010 Pulse Generators Due to Memory Corruption

    Boston Scientific is recalling approximately 12,450 SQ-RX 1010 Pulse Generators because memory corruption may cause the device to deliver an atypical amount of energy.

    Product
    SQ-RX 1010 Pulse Generator, Rx. Product Usage: The S-ICD system is intended to provide defibrillation therapy for the treatment of life-threatening ventricular tachyarrhythmias in patients who do not have symptomatic bradycardia, incessant ventricular tachycardia, or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3037-2017·2017-08-23

    Boston Scientific Recalls Emblem S-ICD Devices Due to Energy Delivery Risk

    Boston Scientific is recalling approximately 16,750 Emblem S-ICD devices because they may deliver atypical energy levels due to internal memory corruption.

    Product
    EMBLEM S-ICD, Model A209, Subcutaneous Implantable Cardioverter Defibrillator, RX. Product Usage: The S-ICD system is intended to provide defibrillation therapy for the treatment of life-threatening ventricular tachyarrhythmias in patients who do not have symptomatic…
    Category
    Medical Device
    Distribution
    Distributed nationwide