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.

45751–45775 of 73832

  • ModerateFDA (Devices)·Z-0318-2017·2016-11-02

    Pentax Video Gastroscope Recall for Updated Operation and Reprocessing Instructions

    Pentax of America Inc is recalling video gastroscopes to provide customers with the most recent Operation and Reprocessing Instructions (IFUs).

    Product
    Pentax Video Gastroscope is intended to be used with a Pentax video processor (including light source), documentation equipment, monitor, EndoTherapy Device such as a Biopsy Forceps, and other ancillary equipment for endoscopy and endoscopic surgery within the upper digestive…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0358-2017·2016-11-02

    Wilton Silver Airbrush Color Recalled for Potential Mold and Bacteria

    Wilton Brands is recalling 17,670 bottles of Silver Airbrush Color found to contain mold, yeast, or bacteria. The product was distributed nationwide in the U.S. and Canada.

    Product
    Wilton Silver Airbrush Color, Net Wt 0.64 FL OZ (19 mL)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0317-2017·2016-11-02

    Zimmer Biomet Recalls Patellofemoral Joint Prosthesis Milling Handpieces

    Zimmer Biomet is recalling 703 Patellofemoral Joint Prosthesis Milling Handpieces because they may be inoperable due to lack of preventative maintenance, potentially delaying surgery.

    Product
    Zimmer¿ Gender Solutions" Patellofemoral Joint Prosthesis Milling Handpiece
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0299-2017·2016-11-02

    Keystone Dental PrimaConnex Straight Implant Recall Due to Cover Screw Mismatch

    Keystone Dental Inc. is recalling 55 units of PrimaConnex Straight Implants because small diameter cover screws were packaged with regular diameter implants.

    Product
    Keystone Dental PrimaConnex¿ Straight Implant TC, RD Internal Connection 4.0 x 11.5mm. Product code:15613K Implants are intended for use in partially or fully edentulous mandibles and maxillae, in support of single or multiple-unit restorations includ-ing; cement retained…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0298-2017·2016-11-02

    TZ Medical Recalls Mis-Labeled Neptune Plus Hemostatic Pads

    TZ Medical is recalling Neptune Plus hemostatic pads because the labels incorrectly state they include an antimicrobial barrier.

    Product
    Neptune Plus (Hemostatic Pad), Part Numbers: 8870-03 Neptune Pad is used to promote the rapid control of bleeding and provide hemostasis for lacerations, abrasions, vascular access sites and following surgical incision. It can be used to achieve hemostasis at the skin surface…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0319-2017·2016-11-02

    Siemens CMV IgM Assay Recalled for Increased Imprecision

    Siemens Healthcare Diagnostics is recalling IMMULITE CMV IgM Assay kits due to reported increases in imprecision and high coefficient of variation (CV) values.

    Product
    IMMULITE/ IMMULITE 1000 Systems CMM CMV IgM Assay, REF/Catalog Number LKCM1(D) - 100 tests (US), Siemens Material Number (SMN) 10370301 (US), Unique Device Identification Number (UDI) 00630414985718 (US); and REF/Catalog Number LKCM1 - 100 tests (OUS); SMN 10381296 (OUS), UDI…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0281-2017·2016-11-02

    Bob's Red Mill Guar Gum Recalled for Misidentified Ingredient

    Bob's Red Mill is voluntarily recalling one lot of Guar Gum due to the inclusion of a misidentified ingredient, hydroxyethylcellulose.

    Product
    Label reads in part "*** Bob's Red Mill *** PREMIUM GUAR GUM SUPERB GLUTEN FREE THICKENER & BINDER *** NET WT 8 OZ ***" Product is packaged in multilayered flexible film with multiple colors. Firm brand name is printed in red. Case contains 8/8 oz. packages. UPC 0…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0356-2017·2016-11-02

    Wilton Black Airbrush Color Recalled for Mold, Yeast, or Bacteria

    Wilton Brands is recalling 16,446 bottles of Black Airbrush Color found to contain mold, yeast, or bacteria. The product was distributed nationwide in the U.S. and Canada.

    Product
    Wilton Black Airbrush Color, Net Wt 0.64 FL OZ (19 mL)
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0115-2017·2016-11-02

    Invokamet Recalled for Incorrect or Missing Package Insert Labeling

    Janssen Ortho L.L.C. is recalling Invokamet tablets because Xarelto prescribing information outserts may be affixed to the bottles instead of the correct Invokamet inserts.

    Product
    INVOKAMET — INVOKAMET (CANAGLIFLOZIN AND METFORMIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0313-2017·2016-11-02

    Ortho-Clinical Diagnostics Recalls VITROS HBsAg Controls Due to Performance Drift

    Ortho-Clinical Diagnostics is recalling VITROS HBsAg Controls because signal/cutoff results may increase during the 5-day reconstituted timeframe, potentially affecting performance monitoring.

    Product
    VITROS Immunodiagnostic Products HBsAg Controls, Product Code 6800598 For in vitro diagnostic use only. For use in monitoring the performance of the VITROS ECi/ECiQ Immunodiagnostic Systems, the VITROS 3600 Immunodiagnostic System and the VITROS 5600 Integrated System when…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16E082000·2016-11-01

    Omix Ada Recalls Replacement Steering Sector Shafts for Early Jeeps

    Omix Ada is recalling 344 replacement steering sector shafts for early Willys and Jeep vehicles due to incomplete heat treatment that may cause premature failure.

    Product
    STEERING:GEAR BOX:SHAFT SECTOR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V795000·2016-11-01

    Spartan Motors Recalls Transit Bus Chassis Cabs Due to Exhaust Fire Risk

    Spartan Motors is recalling 245 model year 2011-2017 Transit Bus Chassis Cabs because a disconnecting exhaust tube may expose the floor to high heat, increasing fire risk.

    Product
    SPARTAN MOTORS — SPARTAN MOTORS TRANSIT BUS CHASSIS CAB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17023·2016-11-01

    Kikkerland Teapots with Bamboo Stands Recalled for Fire Hazard

    Kikkerland Design is recalling teapots with bamboo stands because the stands can catch fire. No injuries have been reported.

    Product
    Kikkerland and Cost Plus World Market brand teapots with bamboo stands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V792000·2016-10-31

    Mitsubishi Recalls Outlander Sport Vehicles for Wiper Motor Corrosion Risk

    Mitsubishi is recalling 2011-2015 Outlander Sport vehicles because water leaks can corrode the wiper motor, potentially causing loss of visibility and increasing crash risk.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V791000·2016-10-31

    Mitsubishi Recalls Outlander Vehicles for Wiper Link Corrosion Risk

    Mitsubishi is recalling 2007-2013 Outlander vehicles because water intrusion can corrode the wiper link, potentially causing the wipers to stop working and reducing visibility.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V788000·2016-10-28

    Mazda Recalls 2010-2011 Tribute Vehicles for Fuel Leak Risk

    Mazda is recalling 2010-2011 Tribute vehicles because a cracked fuel delivery module may leak fuel, increasing the risk of fire.

    Product
    MAZDA — MAZDA TRIBUTE, TRIBUTE HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide