The Recall Desk

State

Northern Mariana Islands product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

37051–37075 of 73761

  • SevereNHTSA·18V585000·2018-09-08

    Trailstar Recalls 2019 Dump Trailers Due to Wheel Separation Risk

    Trailstar is recalling 2019 Dump trailers because improperly installed wheel end nuts may cause the wheel to separate from the axle, increasing crash risk.

    Product
    TRAILSTAR — TRAILSTAR DUMP TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V602000·2018-09-08

    REV Recalls 2017-2018 Ambulances with Whelen Brake Light Wiring Defect

    REV Ambulance Group is recalling 2017-2018 ambulances equipped with Whelen accessory brake lights that may illuminate without the brake pedal being pressed.

    Product
    MARQUE — MARQUE, MCCOY MILLER, ROAD RESCUE TYPE III, TYPE I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V595000·2018-09-07

    GM Recalls 2014-2016 Cadillac CTS for Seat Heater Fire Risk

    General Motors is recalling 2014-2016 Cadillac CTS vehicles because damaged front seat heaters may overheat and cause a fire when the car is remotely started.

    Product
    CADILLAC — CADILLAC CTS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V598000·2018-09-07

    Navistar Recalls 2019 IC Bus School Buses Due to Brake Defect

    Navistar is recalling 2019 IC Bus CE and RE school buses because a parking brake component may be improperly crimped, causing air leaks and increased stopping distances.

    Product
    IC BUS — IC BUS CESB, RESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V597000·2018-09-07

    Navistar Recalls 2019 International and IC Bus Vehicles for Brake Defect

    Navistar is recalling 2,089 2019 International and IC Bus vehicles because a brake chamber defect may cause air leaks, increasing stopping distance and crash risk.

    Product
    INTERNATIONAL — INTERNATIONAL, IC BUS LT, HX, WORKSTAR, DURASTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V599000·2018-09-07

    Honda Recalls 2017 Acura NSX for Brake Light Circuit Defect

    Honda is recalling 793 2017 Acura NSX vehicles because road vibrations may loosen screws, causing the center brake light to fail and increasing crash risk.

    Product
    ACURA — ACURA NSX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V601000·2018-09-07

    Nissan Recalls Murano, Maxima, Pathfinder, and QX60 for Brake Fire Risk

    Nissan is recalling specific 2015-2018 Murano, Maxima, Pathfinder, and 2017 QX60 vehicles because brake fluid leaks may cause electrical shorts and fires.

    Product
    NISSAN — NISSAN, INFINITI MURANO, QX60, MAXIMA, PATHFINDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V586000·2018-09-07

    GM Recalls 2015 SUVs and Trucks for Electric Power Steering Software Issue

    General Motors is recalling 2015 Chevrolet, GMC, and Cadillac vehicles because electric power steering assist may momentarily be lost and then suddenly return, increasing crash risk.

    Product
    CHEVROLET — CHEVROLET, GMC, CADILLAC TAHOE, SUBURBAN, YUKON, SILVERADO 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V594000·2018-09-07

    AEV Traumahawk Ambulances Recalled for Brake Light Wiring Defect

    Halcore Group is recalling 2017-2018 AEV Traumahawk ambulances because Whelen accessory brake lights may illuminate without the brake pedal being pressed, potentially confusing other drivers.

    Product
    AEV — AEV TRAUMAHAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·18V596000·2018-09-07

    Micro Bird Recalls 2018 School Buses for Missing Seat Warning Labels

    Micro Bird is recalling 252 2018 MB II school buses because certain child restraint seats are missing warning labels, which may lead to improper use and injury.

    Product
    MICRO BIRD — MICRO BIRD MB II SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V593000·2018-09-06

    Nissan Recalls 2019 Infiniti QX50 for Knee Air Bag Cover Defect

    Nissan is recalling 2019 Infiniti QX50 vehicles because the passenger-side knee air bag cover may separate unexpectedly in cold crashes, increasing injury risk.

    Product
    INFINITI — INFINITI QX50
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1162-2018·2018-09-05

    Auro Pharmacies Recalls Methyl-Cobalamin Injectable Due to Sterility Concerns

    Auro Pharmacies is recalling 81 vials of Methyl-Cobalamin injectable because processes and equipment were inadequate to assure sterility.

    Product
    Methyl-Cobalamin injectable, 10 mg/mL, 30 mL Multiple Dose vial, Rx only, Central Drugs Compounding Pharmacy, 520 W. La Habra Blvd, La Habra, CA 90631
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2951-2018·2018-09-05

    Haemonetics OrthoPAT Reservoirs Recalled Due to Missing Cannula

    Haemonetics is recalling 348 OrthoPAT QuickConnect Reservoirs because a missing cannula prevents blood from being emptied and processed.

    Product
    Haemonetics¿ OrthoPAT¿ System-OPAT QuickConnect Reservoirs. Product Code: OPT-R-1000 The OrthoPAT orthopedic perioperative autotransfusion system indicated for use to salvage RBCs from blood lost intraoperatively and postoperatively during surgical procedures
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1143-2018·2018-09-05

    Torrent Pharma Recalls Amlodipine, Valsartan, and Hydrochlorothiazide Tablets Due to Impurity

    Torrent Pharma Inc. is recalling specific batches of Amlodipine, Valsartan, and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.

    Product
    Amlodipine, Valsartan and Hydrochlorothiazide Tablets, USP, 10 mg/160 mg/12.5 mg, 30 tablets per bottle, Rx Only, Manufactured by: Torrent Pharmaceuticals LTD., Indrad-382 721, India. NDC: 13668-327-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1140-2018·2018-09-05

    Torrent Pharma Recalls Amlodipine and Valsartan Tablets Due to Carcinogen Impurity

    Torrent Pharma Inc. is recalling specific batches of Amlodipine and Valsartan Tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.

    Product
    Amlodipine and Valsartan Tablets, USP, 5 mg/160 mg, 30 tablets per bottle, Rx Only, Manufactured by: Torrent Pharmaceuticals LTD., Indrad-382 721, India. NDC: 13668-207-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V590000·2018-09-05

    Fabform Recalls 2017-2018 Power Tilt Dump Trailers Due to Hinge Fracture Risk

    Fabform is recalling 2017-2018 Power Tilt dump trailers because welded hinges may fracture, causing the dump box to fall unexpectedly and increasing the risk of injury or death.

    Product
    FABFORM — FABFORM POWER TILT DUMP TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1147-2018·2018-09-05

    Pharmcore Recalls Human Chorionic Gonadotropin Vials Due to Sterility Concerns

    Pharmcore Inc. is recalling 5,718 vials of Human Chorionic Gonadotropin 5000 IU due to a lack of assurance of sterility.

    Product
    Human Chorionic Gonadotropin 5000 IU Vial Lyophilized 1109 East Hallandale Beach Blvd. Hallandale Beach, FL 33009
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1163-2018·2018-09-05

    Auro Pharmacies Recalls Testosterone Injectable Due to Sterility Concerns

    Auro Pharmacies is recalling 43 vials of Testosterone Cypionate/Enanthate injectable because inadequate processes and equipment failed to assure product sterility.

    Product
    Testosterone Cypionate/Enanthate injectable, 126/54 mg/mL, packaged in a) 3 mL and b) 5 mL Multiple Dose vials, Rx only, Central Drugs Compounding Pharmacy, 520 W. La Habra Blvd, La Habra, CA 90631
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1156-2018·2018-09-05

    Auro Pharmacies Recalls CoEnzyme-Q10 Injectable Due to Sterility Concerns

    Auro Pharmacies is recalling 39 vials of CoEnzyme-Q10 injectable because inadequate processes and equipment failed to assure product sterility.

    Product
    CoEnzyme-Q10 injectable, 20 mg/mL, 10 mL Multiple Dose vial, Rx only, Central Drugs Compounding Pharmacy, 520 W. La Habra Blvd, La Habra, CA 90631
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1138-2018·2018-09-05

    Torrent Pharma Recalls Amlodipine and Valsartan Tablets Due to Impurity

    Torrent Pharma Inc. is recalling Amlodipine and Valsartan Tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.

    Product
    Amlodipine and Valsartan Tablets, USP, 5 mg/320 mg, 30 tablets per bottle, Rx Only, Manufactured by: Torrent Pharmaceuticals LTD., Indrad-382 721, India. NDC: 13668-205-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2926-2018·2018-09-05

    Stanbio AC Power Adapter Recall for HemoPoint H2 Meter

    Stanbio Laboratory is recalling AC power adapters for the HemoPoint H2 meter because the adapter plate may crack or detach, exposing live electrical contacts.

    Product
    Stanbio AC power adapter for the HemoPoint H2 meter, Model G3000 series. The firm name on the label for the HemoPoint H2 shows Manufactured by EKF-diagnostic GmbH, Germany.
    Category
    Medical Device
    Distribution
    Distributed nationwide