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.

46701–46725 of 73832

  • ModerateFDA (Devices)·Z-2759-2016·2016-09-14

    Teleflex Horizon Manual-Load Ligating Clip Applier Recalled for Incorrect Etching

    Teleflex Medical is recalling 49 units of Horizon Manual-Load Ligating Clip Appliers due to incorrect etching on the device.

    Product
    WECK¿ Horizon" Manual-Load Ligating Clip Applier, For Medium-Large Size Horizon Ligation Clips Curved Jaw, 11 (28cm), Rx Only, REF 337111, Product Usage: Weck Closure Systems applier has been designed and calibrated for use with specific Horizon, Hemoclip Plus Hemoclip…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1496-2016·2016-09-14

    Teva Recalls Eptifibatide Injection Vials Due to Manufacturing Deviations

    Teva North America is voluntarily recalling 14,661 vials of Eptifibatide Injection due to CGMP deviations. The recall covers lots distributed nationwide and in Puerto Rico.

    Product
    Eptifibatide Injection 75 mg/100 mL (0.75 mg/mL) single use vial, For Intravenous Use Only, Rx Only, Manufactured in Hungary for TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, NDC# 0703-1179-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1490-2016·2016-09-14

    Amerisource Recalls Mispackaged Adderall XR 30 mg Extended-Release Capsules

    Amerisource Health Services is recalling 761 cartons of Adderall XR 30 mg capsules due to unit dose mispackaging where blister cavities may contain more than one capsule.

    Product
    Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate (Mixed Salts of a Single-Entity Amphetamine Product) Extended-Release Capsules CII 30 mg 20 UD Capsules (5 x 4), Rx, Packaged and Distributed by: American Health…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1497-2016·2016-09-14

    Teva Recalls Ondansetron Injection Vials Due to Manufacturing Deviations

    Teva North America is recalling 13,223 vials of Ondansetron Injection USP due to CGMP deviations. The recall covers lots distributed nationwide and in Puerto Rico.

    Product
    Ondansetron Injection USP 40 mg/20 mL (2 mg/mL), Rx Only, Manufactured in Hungary for TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454 NDC # 0703-7226-01 (20 mL- Multi-dose Vial), NDC # 0703-72263-03 (10 Multi-dose Vials per carton)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1480-2016·2016-09-14

    Isomeric Pharmacy Recalls Methylprednisolone Acetate/Lidocaine Injection Due to Sterilization Issue

    Isomeric Pharmacy Solution, LLC is recalling Methylprednisolone Acetate/Lidocaine HCl Injection because excessive sterilization time may cause difficulty resuspending particles.

    Product
    Methylprednisolone Acetate/Lidocaine HCl 40/10 mg/mL Injection, 10 mL multidose vial, sterile. Rx only. Compounded by Isomeric Pharmacy Solutions, Salt Lake City, UT 84109,
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2739-2016·2016-09-14

    GE Healthcare Recalls Centricity Enterprise Archive Software Due to Data Loss Risk

    GE Healthcare is recalling Centricity Enterprise Archive software version 3.0.x due to a potential for data loss when the cache disk is nearly full.

    Product
    Centricity Enterprise Archive is a software product for receiving, archiving and sending of medical data. Qualified system administrators install, monitor and maintain the system. DICOM devices (e.g. modalities, workstations) communicate with the archive using the DICOM protocol…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1488-2016·2016-09-14

    Amerisource Recalls Mispackaged Adderall XR 20 mg Extended-Release Capsules

    Amerisource Health Services is recalling 666 cartons of Adderall XR 20 mg capsules due to unit dose mispackaging where blister cavities may contain more than one capsule.

    Product
    Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate (Mixed Salts of a Single-Entity Amphetamine Product) Extended-Release Capsules, CII 20 mg, 30 UD Capsules (5 x 6), Rx, Packaged and Distributed by: American Health…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2078-2016·2016-09-14

    Nature Made Vitamin D Tablets Recalled for Yeast and Mold

    Pharmavite is recalling specific lots of Nature Made Vitamin D tablets because they may exceed specifications for yeast and mold.

    Product
    Nature Made(R) D3 1000IU, 350 count, UPC 0-31604-04070-3
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2741-2016·2016-09-14

    Arrow Radial Artery Catheterization Kits Recalled for Shipping Labeling Error

    Arrow International Inc. is recalling 690 Radial Artery Catheterization Kits due to a shipping carton labeling error. The kits were distributed to Ohio, Indiana, Tennessee, North Carolina, and Kentucky.

    Product
    Radial Artery Catheterization Kit with Sharps Safety Features Permits access to the peripheral arterial circulation. The safety feature is intended to help minimize the risk of sharps injuries when using the device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2740-2016·2016-09-14

    Arrow Arterial Line Catheterization Kits Recalled for Shipping Labeling Error

    Arrow International Inc. is recalling 690 Arterial Line Catheterization Kits due to a shipping carton labeling error. The kits were distributed nationwide to five states.

    Product
    Arterial Line Catheterization Kit with Sharps Safety Features Permits access to the peripheral arterial circulation or to other small vessels.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V658000·2016-09-13

    Freightliner Trucks Recalled for Brake Caliper Bolt Torque Issues

    Daimler Trucks North America is recalling 2016-2017 Freightliner M2 and 114 SD trucks because brake caliper mounting bolts may be incorrectly torqued, potentially reducing braking ability.

    Product
    FREIGHTLINER — FREIGHTLINER 114SD, BUSINESS CLASS M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16E071000·2016-09-13

    EVS Emergency Vehicle Seats Recalled for Slide Track Defect

    EVS is recalling emergency vehicle seats with Dometic/Atwood slide tracks that may not engage properly, increasing injury risk in a crash.

    Product
    SEATS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V655000·2016-09-13

    Forest River Recalls 2017 Surveyor Trailers Due to Tire Placard Mismatch

    Forest River is recalling 2017 Surveyor recreational trailers because tires and rims may not match the Federal Placard, risking over-inflation and tire failure.

    Product
    FOREST RIVER — FOREST RIVER SURVEYOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V657000·2016-09-13

    Thomas Built Buses Saf-T-Liner C2 School Bus Fuel Leak Recall

    Daimler Trucks North America is recalling 114 model year 2017 Thomas Built Buses Saf-T-Liner C2 school buses due to a potential fuel leak risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V654000·2016-09-12

    FCCC Motorhome Chassis Recall for Brake Signal Defect

    Daimler Trucks is recalling 2013-2016 FCCC XCM, XCR, and XCL motorhome chassis because a brake signal may remain active, causing towed device brakes to drag and potentially overheat.

    Product
    FCCC — FCCC XCL, XCR, XCM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·079-2016·2016-09-10

    MIH Marketing Recalls Meat and Poultry Products Due to Insanitary Conditions

    MIH Marketing and Sales is recalling approximately 662,049 pounds of raw chicken products stored under insanitary conditions, including rodent activity.

    Product
    MIH Marketing and Sales Recalls Meat and Poultry Products Due To Insanitary Conditions
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V653000·2016-09-09

    BMW Recalls M2, M3, and M4 Models for Rear Sub-Frame Bolt Issue

    BMW is recalling specific M2, M3, and M4 vehicles because reused rear sub-frame bolts may loosen, affecting handling and increasing crash risk.

    Product
    BMW — BMW M4, M2, M3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·077-2016·2016-09-08

    Carnival Supermarket Recalls Ground Beef Due To E. Coli O157:H7

    Carnival Supermarket in Chula Vista, California, is recalling approximately 35 pounds of ground beef sold on Sept. 1, 2016, due to possible E. coli O157:H7 contamination.

    Product
    Paradise Valley Market, Inc. (Carnival Supermarket) Recalls Ground Beef Productsdue To Possible E. Coli O157:H7 Adulteration
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V652000·2016-09-08

    Cambli Recalls 2014-2015 Beverage Industry Trailers Due to Brake Defect

    Cambli is recalling 2014-2015 Beverage Industry trailers because improperly machined spring brake valves may delay braking, causing the trailer to roll away.

    Product
    CAMBLI — CAMBLI BEVERAGE INDUSTRY TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V648000·2016-09-08

    Audi Recalls 2017 Q7 Vehicles Due to Electric Power Steering Defect

    Volkswagen Group of America is recalling 2017 Audi Q7 vehicles because the electric power steering control unit may short circuit, causing a loss of steering assist and increasing crash risk.

    Product
    AUDI — AUDI Q7
    Category
    Vehicle
    Distribution
    Distributed nationwide