The Recall Desk

State

Northern Mariana Islands product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

45051–45075 of 73832

  • HighNHTSA·16V930000·2016-12-23

    KME Recalls Fire Trucks Due to Ladder Position Sensor Defect

    Kovatch Mobile Equipment Corp. is recalling certain KME fire trucks because water may leak into the ladder position sensor, increasing the risk of injury.

    Product
    KME — KME PREDATOR SS AERIAL, PREDATOR AERIAL, PREDATOR PANTHER AERIAL, PREDATOR TDA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V950000·2016-12-23

    ARBOC Spirit of Liberty Buses Recalled for Parking Brake Defect

    ARBOC is recalling 2015-2016 Spirit of Liberty transit buses because the parking brake may engage unexpectedly while driving, increasing crash risk.

    Product
    ARBOC — ARBOC SPIRIT OF LIBERTY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V923000·2016-12-22

    Pierce Recalls 2015-2016 Dash CF Emergency Vehicles Due to Fire Risk

    Pierce Manufacturing is recalling 2015-2016 Dash CF emergency vehicles because a defective bracket may damage the starter motor, increasing the risk of a fire.

    Product
    PIERCE — PIERCE DASH CF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V925000·2016-12-22

    Ford Recalls 2016-2017 Vehicles for Turbocharger Oil Leak Fire Risk

    Ford is recalling specific 2016-2017 Taurus, Flex, MKT, and Explorer vehicles because improperly brazed turbocharger tubes may leak oil, increasing fire risk.

    Product
    FORD — FORD, LINCOLN FLEX, TAURUS, MKT, EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V926000·2016-12-22

    KME Predator Aerial Vehicles Recalled for Brake Defect

    KME is recalling certain Predator SS Aerial and Predator Aerial vehicles because rear brakes may engage without the pedal being pressed, increasing crash and fire risk.

    Product
    KME — KME PREDATOR AERIAL, PREDATOR SS AERIAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V928000·2016-12-22

    Volvo Recalls 2013-2017 Trucks Due to Brake System Contamination Risk

    Volvo is recalling certain 2013-2017 VNL, VNM, and 2017 VNX trucks because incorrect software may allow oil and water to contaminate the brake system, potentially affecting braking performance.

    Product
    VOLVO — VOLVO VNM, VNX, VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V927000·2016-12-22

    Volvo Recalls 2017 Trucks Due to Front Wheel Hub Defect

    Volvo is recalling 2017 VHD, VNL, and VNM trucks because front wheel hubs may fail, risking loss of vehicle control.

    Product
    VOLVO — VOLVO VNM, VNL, VHD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V947000·2016-12-22

    Chrysler Recalls 2009 Durango, Aspen, and 2010 RAM 3500 for Air Bag Defect

    Chrysler is recalling specific 2009 Dodge Durango, Chrysler Aspen, and 2010 RAM 3500 vehicles because the driver's air bag inflator may rupture during deployment, posing a risk of serious injury.

    Product
    DODGE — DODGE, CHRYSLER RAM 3500, ASPEN, DURANGO, redundant RAM 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17059·2016-12-22

    4 Sizzle Recalls Promotional Charcoal Grills Due to Fire Hazard

    4 Sizzle LLC is recalling approximately 1,700 wooden barrel-shaped charcoal grills with the Shock Top logo due to a fire hazard. The grills were distributed as promotional items and display enhancers.

    Product
    Charcoal grills
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0189-2017·2016-12-21

    Cantrell Drug Company Recalls Fentanyl Citrate Bags Due to Sterility Concerns

    Cantrell Drug Company is recalling Fentanyl Citrate bags due to a lack of assurance of sterility. The recall affects 2,545 bags distributed nationwide.

    Product
    Fentanyl Citrate 2,500 mcg in 0.9% Sodium Chloride (10 mcg/mL) 250 mL* Bag, Single-Dose Bag, Rx Only, Cantrell Drug Company 7321 Cantrell Road Little Road, AR 72207, NDC 52533-024-61
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0194-2017·2016-12-21

    Cantrell Drug Recalls Hydromorphone Syringes Due to Sterility Concerns

    Cantrell Drug Company is recalling 2,509 single-dose Hydromorphone HCl syringes nationwide due to a lack of assurance of sterility.

    Product
    HYDROmorphone HCl 6 mg/30 mL in 0.9% Sodium Chloride (0.2 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-002-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0202-2017·2016-12-21

    Cantrell Drug Recalls Rocuronium Bromide Syringes Due to Sterility Concerns

    Cantrell Drug Company is recalling 5,067 syringes of Rocuronium Bromide 50 mg/5 mL injection solution nationwide due to a lack of assurance of sterility.

    Product
    Rocuronium Bromide 50 mg/5 mL Injection Solution, 5 mL (10 mg/mL) Single-Dose Syringe, Injection Solution For Slow IV Use, Rx Only, Cantrell Drug Co. 7321 Cantrell Rd. Little Rock, AR 72207, NDC 52533-064-15
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0188-2017·2016-12-21

    Cantrell Drug Recalls Fentanyl Citrate Bags Due to Sterility Concerns

    Cantrell Drug Company is recalling 471 bags of Fentanyl Citrate 1,500 mcg in 0.9% Sodium Chloride due to a lack of assurance of sterility.

    Product
    Fentanyl Citrate 1,500 mcg in 0.9% Sodium Chloride (10 mcg/mL) 150 mL Bag, Single-Dose Bag, Rx Only, Cantrell Drug Company 7321 Cantrell Road Little Road, AR 72207, NDC 52533-024-35
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0191-2017·2016-12-21

    Cantrell Drug Recalls Glycopyrrolate Injection Due to Sterility Concerns

    Cantrell Drug Company is recalling specific lots of Glycopyrrolate injection because the firm cannot assure the sterility of the product.

    Product
    Glycopyrrolate 1 mg/5 mL (0.2 mg/mL) Injection Solution, 5 mL Single-Dose Syringe, For IV Use, Hospital/Office Use Only, Rx Only, Cantrell Drug Co. 7321 Cantrell Rd. Little Rock, AR 72207, NDC 52533-028-15
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0192-2017·2016-12-21

    Cantrell Drug Recalls Heparin Sodium Syringes Due to Sterility Concerns

    Cantrell Drug Company is recalling 1,494 syringes of Heparin Sodium due to a lack of assurance of sterility. The products were distributed nationwide.

    Product
    Heparin Sodium, 1 USP Unit/2 mL (0.5 USP Units/mL) in 0.45% Sodium Chloride, Single-Dose Syringe, Hospital/Office Use Only, Rx Only, Cantrell Drug Co. 7321 Cantrell Rd. Little Rock, AR 72207, NDC 52533-148-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0193-2017·2016-12-21

    Cantrell Drug Recalls Heparin Sodium Bags Due to Sterility Concerns

    Cantrell Drug Company is recalling 150 bags of Heparin Sodium 5,000 USP Units in 0.9% Sodium Chloride due to a lack of assurance of sterility.

    Product
    Heparin Sodium 5,000 USP Units Added to 0.9% Sodium Chloride 1,000 mL* Bag (5 USP units/mL), Single-Dose Bag.,Hospital/Office Use Only, Injection Solution For IV Use, Rx Only, Cantrell Drug Company 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-097-24
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V922000·2016-12-21

    GM Recalls 2016 Buick Envision for Brake Line Cracking Risk

    General Motors is recalling 2016 Buick Envision vehicles because master cylinder brake lines may crack and leak fluid, potentially reducing braking performance.

    Product
    BUICK — BUICK ENVISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0190-2017·2016-12-21

    Cantrell Drug Company Recalls Fentanyl and Bupivacaine Bags for Sterility Concerns

    Cantrell Drug Company is recalling specific lots of Fentanyl Citrate and Bupivacaine HCl bags due to a lack of assurance of sterility.

    Product
    Fentanyl Citrate 2 mcg/mL & Bupivacaine HCl 0.125% in 0.9% Sodium Chloride, 100 mL* Bag, Epidural Use Only, Single-Dose Bag, Hospital/Office Use Only, Rx Only, Cantrell Drug Company 7321 Cantrell Road Little Road, AR 72207, NDC 52533-080-75
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0198-2017·2016-12-21

    Cantrell Drug Recalls Midazolam HCl Syringes Due to Sterility Concerns

    Cantrell Drug Company is recalling 37 syringes of Midazolam HCl 50 mg/50 mL due to a lack of assurance of sterility. The product was distributed nationwide.

    Product
    Midazolam HCl 50 mg/50 mL in 0.9% Sodium Chloride (1 mg/mL), Single-Dose Syringe, Hospital/Office Use Only, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-001-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0187-2017·2016-12-21

    Cantrell Drug Recalls Calcium Chloride Injection Due to Sterility Concerns

    Cantrell Drug Company is recalling 645 vials of Calcium Chloride Injection Solution because the firm cannot assure the sterility of the product.

    Product
    Calcium Chloride, (1 g/10 mL) Injection Solution 10 mL, 10% Single-Dose Vial, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0199-2017·2016-12-21

    Cantrell Drug Recalls Morphine Sulfate Bags Due to Sterility Concerns

    Cantrell Drug Company is recalling 1,748 bags of Morphine Sulfate 1 mg/mL due to a lack of assurance of sterility. The product was distributed nationwide.

    Product
    Morphine Sulfate 1 mg/mL in 0.9% Sodium Chloride, 100 mL Bag, Single-Dose Bag, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-160-75
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0195-2017·2016-12-21

    Cantrell Drug Recalls Hydromorphone Syringes Due to Sterility Concerns

    Cantrell Drug Company is recalling 935 vials of Hydromorphone HCl 50 mg/50 mL single-dose syringes due to a lack of assurance of sterility.

    Product
    HYDROmorphone HCl 50 mg/50 mL in 0.9% Sodium Chloride (1 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-006-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0184-2017·2016-12-21

    Cantrell Drug Recalls Calcium Chloride Bags Due to Sterility Concerns

    Cantrell Drug Company is recalling 80 bags of Calcium Chloride 1 g/50 mL due to a lack of assurance of sterility.

    Product
    Calcium Chloride 1 g/50 mL* Added to 5% Dextrose (20 mg/mL)*, Single-Dose Bag, Rx Only, Hospital/Office Use Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-175-37
    Category
    Drug
    Distribution
    Distributed nationwide