The Recall Desk

State

Northern Mariana Islands product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

59326–59350 of 73856

  • LowFDA (Devices)·Z-0965-2014·2014-02-19

    Bio-Rad D-10 Hemoglobin Testing System Software Recall

    Bio-Rad is recalling D-10 Dual Program software due to incorrect cartridge count updates when switching programs.

    Product
    D-10 Dual Program, which contains Update Kit D-10 A1c program diskette. United States; Bio-Rad Laboratories, Hercules, CA 94547 The Bio-Rad D-10 Hemoglobin Testing System provides an integrated method for the separation and determination of the relative percent of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1083-2014·2014-02-19

    Bracco Recalls VoLumen Barium Sulfate Suspension Due to Stability Failure

    Bracco Diagnostics Inc is recalling VoLumen Barium Sulfate Suspension because the product failed stability testing for preservative content.

    Product
    VoLumen Barium Sulfate Suspension (0.1 % w/v, 0.1 ww/w), 450 mL bottle, Rx Only. Manufactured by E-Z-EM Canada Inc. a subsidiary or E-Z-EM, Inc. Lake Success, NY 11042. NDC 32909-945-03.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V060000·2014-02-18

    Diamond Coach Recalls 2009-2010 VIP/PT Transit Buses for Fire Risk

    Diamond Coach is recalling 2009-2010 VIP/PT transit buses because voltage spikes may damage door actuator circuit boards, increasing the risk of a fire.

    Product
    VIP/PT — VIP/PT 2800, 3200, 3201, 2200
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14E004000·2014-02-18

    Aisin Automatic Transmission Recall for Power Loss Risk

    Aisin World Corp. of America is recalling specific automatic transmissions for Isuzu and Chrysler vehicles due to a loose snap ring that may cause a loss of power transfer.

    Product
    POWER TRAIN:AUTOMATIC TRANSMISSION recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V086000·2014-02-18

    PACCAR Recalls Kenworth and Peterbilt Trucks Due to Fire Risk

    PACCAR is recalling specific 2014-2015 Kenworth and Peterbilt tractor trailers because condensation in the intake manifold may freeze, causing exhaust flames and increasing the risk of fire or burn injury.

    Product
    KENWORTH — KENWORTH, PETERBILT T660, T800, W900, T440
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V069000·2014-02-18

    Gulf Stream GT GulfTran Shuttle Recall for Door Actuator Fire Risk

    Gulf Stream Coach is recalling 2011 GT GulfTran shuttles because voltage spikes may damage door actuator circuit boards, increasing the risk of a fire.

    Product
    GULF STREAM — GULF STREAM GT GULFTRAN SHUTTLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14715·2014-02-18

    Club Car Recalls Precedent I2 Golf Vehicles Due to Fall Hazard

    Club Car is recalling about 1,800 Precedent I2 golf and transport vehicles because the passenger-side hip restraint can fracture, posing a fall hazard.

    Product
    Precedent I2 golf and transport vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14106·2014-02-18

    LEM 5-Tray Food Dehydrators Recalled for Electrical Shock Hazard

    LEM Products is expanding a recall of 5-tray food dehydrators due to damaged wiring that poses a shock hazard. Consumers should stop using the units and contact the company for repair.

    Product
    5-Tray Dehydrators with Digital Timers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·015-2014·2014-02-15

    Nutriom Recalls Dried Egg Products Due to Possible Salmonella Contamination

    Nutriom LLC is recalling approximately 226,710 pounds of dried egg products due to possible Salmonella contamination. The products were shipped nationwide, to U.S. military installations, and to Canada.

    Product
    Washington Firm Recalls Dried Egg Products Due to Possible Salmonella Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·14E003000·2014-02-14

    Cummins Westport Engine Recall for Intake Manifold Sensor Defect

    Cummins is recalling Westport ISL G and ISX12 G engines because condensation in the intake manifold may freeze and interfere with the pressure sensor, potentially causing exhaust fires or burns.

    Product
    ENGINE AND ENGINE COOLING:ENGINE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V056000·2014-02-14

    Honda Recalls 2013 CB500 and CBR500 Motorcycles for Engine Bolt Defect

    Honda is recalling 2013 CB500 and CBR500 motorcycles because rocker arm shaft retaining bolts may loosen, causing oil leaks and potential engine stalls.

    Product
    HONDA — HONDA CBR500RA, CB500XA, CBR500R, CB500FA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1054-2014·2014-02-12

    B. Braun Recalls Cefepime Injection Due to Visible Organic Particulate Matter

    B. Braun Medical Inc. is recalling 18,936 containers of Cefepime Hydrochloride and Dextrose Injection due to the presence of visible organic particulate matter.

    Product
    CEFEPIME HYDROCHLORIDE AND DEXTROSE — CEFEPIME HYDROCHLORIDE AND DEXTROSE (CEFEPIME HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1061-2014·2014-02-12

    Teva Recalls Valacyclovir Tablets Due to Potential Foreign Tablet Fragments

    Teva Pharmaceuticals USA is recalling Valacyclovir Hydrochloride 1 g tablets because bottles may contain fragments of Pravastatin tablets.

    Product
    Valacyclovir Hydrochloride Tablets, 1 g, 30 count bottle, Rx only manufactured in Israel by Teva Pharmaceuticals Ind., LTD, Jerusalem, Israel, Manufactured for Teva Pharmaceuticals USA, Sellersville, PA. NDC #0093-7259-56
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1057-2014·2014-02-12

    Baxter Recalls Nitroglycerin Injection Due to Particulate Matter

    Baxter Healthcare is recalling 49,932 vials of Nitroglycerin in Dextrose Injection because particulate matter was found in one vial.

    Product
    NITROGLYCERIN IN DEXTROSE — NITROGLYCERIN IN DEXTROSE (NITROGLYCERIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0905-2014·2014-02-12

    Medtronic Aquamantys3 Pump Generator Recalled for Electrical Safety Defect

    Medtronic is recalling 242 Aquamantys3 Pump Generators because internal protection circuitry may fail, exposing patients to DC voltage during surgery.

    Product
    Medtronic Advanced Energy Aquamantys3 Pump Generator; Product Catalog Number: 10-1357 (Generator assembly), 40-404-1(as shipped, including accessories) The Aquamantys3 System combines radio frequency (RF) energy and saline to reduce blood loss during and after surgical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V052000·2014-02-12

    Nissan Recalls 2012-2014 Frontier Vehicles for Wiring Fire Risk

    Nissan is recalling 2012-2014 Frontier vehicles because an incorrectly installed circuit breaker may cause a wire harness to contact a metal bolt, potentially leading to an electrical short and fire.

    Product
    NISSAN — NISSAN FRONTIER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1066-2014·2014-02-12

    Apothecure Recalls Sterile Compounded Products Due to Sterility Assurance Concerns

    Apothecure, Inc. is recalling all lots of sterile compounded products within expiry due to lack of sterility assurance identified during an FDA inspection.

    Product
    The firm is recalling all lots of sterile products compounded by the pharmacy that are within expiry.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0908-2014·2014-02-12

    Medtronic Mosaic Aortic Obturator Recalled for High Transvalvular Gradients

    Medtronic is recalling Mosaic Aortic Obturators used with Mosaic Porcine Aortic Bioprostheses due to higher-than-expected transvalvular gradients after implant.

    Product
    Product Name: Model 7305- Mosaic Aortic Obturator The Mosaic Aortic Obturators are used with the Mosaic Porcine Aortic Bioprostheses.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0918-2014·2014-02-12

    Edwards Lifesciences Recalls 26mm Transcatheter Heart Valve Crimpers

    Edwards Lifesciences is recalling two lots of 26mm transcatheter heart valve crimpers because they may not open fully, potentially preventing proper valve preparation.

    Product
    Crimper Model 9100CR26 The Crimper is indicated for use in preparing the Edwards SAPIEN Transcatheter Heart Valve for implantation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0931-2014·2014-02-12

    CareFusion Recalls Trifurcated Extension Sets Due to Potential Component Leak

    CareFusion 303, Inc. is recalling Trifurcated Extension Sets (models ME 1224 and MP 9230) because a defect in the trifurcated component could result in a leak.

    Product
    Trifurcated Extension Set, model no. ME 1224. Trifurcated Extension Set, model no. MP 9230.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0937-2014·2014-02-12

    ITC-Nexus Dx Recalls Hemochron Jr. Citrate APTT Cuvettes for Inaccurate Results

    ITC-Nexus Dx is recalling Hemochron Jr. Citrate APTT Cuvettes because they may produce higher than expected results in normal individuals.

    Product
    Hemochron Jr. Citrate APTT Cuvette 510(k) K014008 A unitized microcoagulation test intended to be used in performing a quantitative, one -stage APTT. The citrate APTT test is used for evaluation of low doses of heparin anticoagulant (up to 1.5 units/mL), depending upon…
    Category
    Medical Device
    Distribution
    Distributed nationwide