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.

39801–39825 of 73764

  • SevereNHTSA·18V101000·2018-02-08

    Micro Bird Recalls T-Series Transit Buses Due to Seat Belt Anchor Defect

    Micro Bird is recalling 2015-2018 T-Series transit buses because seat belt attachments may not remain secured to the floor in a crash, increasing injury risk.

    Product
    MICRO BIRD — MICRO BIRD T-SERIES TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18723·2018-02-08

    Poppin Recalls Pitch Rolling Chairs Due to Fall Hazard

    Poppin is recalling about 2,800 Pitch rolling chairs because the seat plate can break and detach, posing a fall hazard. No injuries have been reported.

    Product
    Pitch rolling chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V098000·2018-02-08

    Chrysler Recalls 2017 Jeep Wrangler and Dodge Caravan for Brake Switch Defect

    Chrysler is recalling 2017 Jeep Wrangler and Dodge Caravan vehicles because brake switches may malfunction, allowing the vehicle to shift out of Park without the brake pedal being pressed.

    Product
    JEEP — JEEP, DODGE WRANGLER, CARAVAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18095·2018-02-08

    Husqvarna Recalls Zero Turn Riding Mowers Due to Fire Hazard

    Husqvarna is recalling about 7,100 residential zero turn riding mowers because a fuel line defect can cause leaks and fire. No injuries have been reported.

    Product
    Residential zero turn riding mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V100000·2018-02-08

    RAM Trucks Recalled for Transmission Shift Interlock Defect

    Chrysler is recalling 2017-2018 RAM trucks because the brake pedal interlock may fail, allowing the vehicle to shift out of Park without the brake pedal being pressed.

    Product
    RAM — RAM 3500, 4500, 1500, 5500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0247-2018·2018-02-07

    Blue Pearl Capsules Recalled for Undeclared Sildenafil

    Blue Fusion Natural is recalling Blue Pearl capsules because FDA analysis found undeclared sildenafil, an unapproved drug for erectile dysfunction.

    Product
    BLUE PEARL capsules, 500mg, 1-count packets, Distributed by Blue Pearl Long Beach, CA UPC 8 4704600978 5
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0472-2018·2018-02-07

    Clopidogrel Tablets Recalled Due to Simvastatin Labeling Error

    International Laboratories, LLC is recalling Clopidogrel Tablets 75 mg because bottles were found containing Simvastatin Tablets 10 mg.

    Product
    Clopidogrel Tablets, USP 75 mg, 30-count bottles, Rx only, Packaged for: International Laboratories, LLC St. Petersburg, FL 33710, NDC 54458-888-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0267-2018·2018-02-07

    Medline Incision and Drainage Tray Kit Recalled for Subpotent Iodine

    Medline is recalling Incision and Drainage Tray Kits because the Povidone-Iodine prep pads contain less iodine than labeled.

    Product
    Medline Incision and Drainage Tray Kit, Sterile, Single use only. Packaged in USA for Medline Industries, Inc., Mundelein, IL 60060
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0306-2018·2018-02-07

    Medline Anesthesia Kit Recalled for Subpotent Povidone-Iodine Concentration

    Medline Industries is recalling 60 cases of Anesthesia Kits because the Povidone-Iodine prep pads contain less iodine than the label claims.

    Product
    Medline Anesthesia Kit, Single Use Only. Packaged in Mexico by Medline Industries, Inc., Northfield, IL 60093
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0311-2018·2018-02-07

    Medline Recalls Suture Removal Kits with Subpotent Iodine Concentration

    Medline Industries is recalling Suture Removal Kits because the iodine concentration is below the label claim.

    Product
    Professional Hospital Supply Suture Removal Kit, Sterile, Single Use Only. Packaged in Mexico for Professional Hospital Supply, Inc., 41980 Winchester Rd., Temecula, CA 92590
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0299-2018·2018-02-07

    Medline Recalls IV Start Kits With Subpotent Iodine Concentration

    Medline Industries is recalling IV Start Kits because the iodine concentration in the prep pads is below the labeled claim.

    Product
    Medical Equipment Affiliates IV Start Kit, Sterile, Single Use Only. Packaged in Mexico for Medical Equipment Affiliates., Tahlequah, OK 74464
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0274-2018·2018-02-07

    Medline Incision and Drainage Tray Kits Recalled for Subpotent Iodine

    Medline Industries is recalling sterile incision and drainage tray kits because the povidone-iodine prep pads contain less iodine than labeled.

    Product
    Medline INCISION AND DRAINAGE TRAY Kit, Sterile, Single use only. Packaged in Mexico for Medline Industries, Inc., Mundelein, IL 60060
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0270-2018·2018-02-07

    Medline Wound Closure Tray Recalled for Subpotent Iodine Concentration

    Medline Industries is recalling 80 cases of Wound Closure Trays because the iodine concentration in the prep pads is below the labeled claim of 0.85%.

    Product
    Medline Wound Closure Tray, Sterile, Single use only. Packaged in Mexico for Medline Industries, Inc., Northfield, IL 60093
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0298-2018·2018-02-07

    Medline Recalls IV Start Kits With Subpotent Iodine Concentration

    Medline Industries is recalling IV Start Kits because the iodine concentration in the prep pads is below the labeled claim of 0.85%.

    Product
    Medline IV Start Kit, Sterile, Single Use Only. Packaged in Mexico for Medline Industries, Inc., Northfield, IL 60093
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0268-2018·2018-02-07

    Medline I&D Tray Kits Recalled for Subpotent Povidone-Iodine Concentration

    Medline Industries is recalling I&D Tray Kits because the Povidone-Iodine prep pads contain less iodine than the label claims.

    Product
    Medline I&D Tray Kit, Sterile, Single use only. Packaged in Mexico for Medline Industries, Inc., Mundelein, IL 60060
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0295-2018·2018-02-07

    Medline Recalls Povidone-Iodine Prep Pads Due to Subpotent Iodine Levels

    Medline Industries is recalling sterile Povidone-Iodine prep pads because the iodine content is below the labeled 0.85% claim.

    Product
    Medline General Purpose Instrument Set, Sterile, Single Use Only. Packaged in Mexico for Medline Industries, Inc., Mundelein, IL 60060
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0275-2018·2018-02-07

    Medline Circumcision Tray Kit Recalled for Subpotent Iodine Concentration

    Medline Industries is recalling Circumcision Tray Kits because the iodine concentration in the prep pads is below the labeled claim.

    Product
    Medline Circumcision Tray Kit, Sterile, Single use only. Packaged in Mexico for Medline Industries, Inc., Northfield, IL 60093
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0261-2018·2018-02-07

    Medline CNTRL Line Removal Kit Recalled for Subpotent Iodine Content

    Medline Industries is recalling CNTRL Line Removal Kit Scripps because the iodine content is below the label claim.

    Product
    Medline CNTRL Line Removal Kit Scripps. Packaged in USA for Medline Industries, Inc., Northfield, IL 60093
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0294-2018·2018-02-07

    Medline Suture Removal Kit Recalled for Subpotent Iodine Concentration

    Medline Industries is recalling Suture Removal Kits because the iodine concentration is below the label claim of 0.85%.

    Product
    Medline Suture Removal Kit, Sterile, Single Use Only. Packaged in Mexico for Medline Industries, Inc., Mundelein, IL 60060
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0289-2018·2018-02-07

    Medline Suture Removal Tray Recalled for Subpotent Iodine Concentration

    Medline Industries is recalling Suture Removal Trays because the Povidone-Iodine prep pads contain less iodine than the label claims.

    Product
    Medline Suture Removal Tray, Sterile, Single Use Only. Packaged in Mexico for Medline Industries, Inc., Mundelein, IL 60060
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0316-2018·2018-02-07

    Medline Abdominal Surgery Packs Recalled for Low Iodine Content

    Medline Industries is recalling Abdominal Surgery II Packs because the iodine content in the prep pads is below the label claim.

    Product
    Medline Abdominal Surgery II Pack-LF, Sterile, Single Use Only. Packaged in USA for Medline Industries, Inc., Northfield, IL 60093
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0314-2018·2018-02-07

    Medline Skin Stapler RMVR Recalled for Subpotent Iodine Concentration

    Medline Industries is recalling Skin Stapler RMVR trays because the iodine concentration in the prep pads is below the labeled claim.

    Product
    Medline Skin Stapler RMVR, Tray Sterile, Single Use Only. Packaged in Mexico for Medline Industries, Inc., Mundelein, IL 60060
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0302-2018·2018-02-07

    Medline Incision and Drainage Tray Recalled for Subpotent Iodine

    Medline is recalling Incision and Drainage Trays because the Povidone-Iodine prep pads contain less iodine than labeled.

    Product
    Medline Incision and Drainage Tray, Sterile, Single Use Only. Packaged in Mexico by Medline Industries, Inc., Mundelein, IL 60060
    Category
    Medical Device
    Distribution
    Distributed nationwide