The Recall Desk

State

Northern Mariana Islands product recalls

73,598 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 73,598 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29726–29750 of 73621

  • SevereFDA (Drugs)·D-0850-2020·2020-02-26

    NCS Healthcare Recalls Glycopyrrolate Tablets Due to Impurity Failure

    NCS Healthcare of Kentucky Inc is recalling 6,929 blister cards of Glycopyrrolate Tablets, USP, 1 mg, due to high out-of-specification results for an unknown impurity.

    Product
    Glycopyrrolate Tabs, USP, 1 mg, 30-count unit dose blister card, FOR INSTITUTIONAL USE ONLY, Rx Only, Packaged by Vangard, Glasgow, KY 42141; NDC 0615-8170-39.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0705-2020·2020-02-26

    ABH Nature's Products Recalls All Dietary Supplements for cGMP Violations

    ABH Nature's Products Inc. is recalling all dietary supplements under a consent decree because they were prepared, packed, or held in violation of current good manufacturing practice regulations.

    Product
    All Dietary Supplement manufactured and distributed by ABH Nature's Products Inc.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1333-2020·2020-02-26

    Siemens Uroskop Omnia max Recalled for Collision Control Override Risk

    Siemens is recalling 192 Uroskop Omnia max devices because a bypass key can override collision controls, creating a risk of collision with obstacles or persons.

    Product
    Uroskop Omnia max, Model No. 10762473 - Product Usage: Uroskop Omnia Max is a device intended to visualize anatomical structures by converting an Xray pattern into a visible image. The system is designed primarily for urological diagnosis and the support of urological…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1286-2020·2020-02-26

    Recall of Polysorb Sutures Due to Potential Packaging Integrity Issues

    Covidien LLC is recalling specific lots of Polysorb Braided Absorbable Sutures due to potential packaging integrity issues that could impact sterility.

    Product
    Polysorb Braided Absorbable Suture 2-0 VIOLET 30" V-20, Item Code GL123 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0708-2020·2020-02-26

    Dragonfly Botanicals Breathe Deep Recalled for Internal Use of Coltsfoot

    Green Water, LLC is recalling Dragonfly Botanicals Breathe Deep dietary supplements because they contain Coltsfoot, which is not to be used internally.

    Product
    Dragonfly Botanicals Full spectrum Breathe Deep 1000mg/oz Dietary Supplement, sold in 0.5 oz, 1 oz, 2 oz, and 4 oz amber glass bottles with dropper.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0707-2020·2020-02-26

    Taspen's Organics Breathe Easy Herbal Tincture Recalled for Coltsfoot

    Green Water, LLC is recalling Taspen's Organics Breathe Easy Herbal Tincture because it contains Coltsfoot, which is not to be used internally.

    Product
    Taspen's Organics Breathe Easy Herbal Tincture Dietary Supplement, sold in 1 oz, 2 oz, and 4 oz amber glass bottles with dropper.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1290-2020·2020-02-26

    Polysorb Braided Absorbable Suture Recalled for Packaging Integrity Issues

    Covidien LLC is recalling specific lots of Polysorb Braided Absorbable Suture due to potential packaging integrity issues that may impact the humidity or sterility barrier.

    Product
    Polysorb Braided Absorbable Suture 3/0 30" UNDYED V-20, Item Code GLS322 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0724-2020·2020-02-26

    Safeway Chocolate Buttercreme Base Recalled for Plastic Polymer Contamination

    CSM Bakery Products is recalling 45 lb. boxes of Safeway Chocolate Buttercreme Base because pieces of plastic polymer were introduced into the sugar system.

    Product
    45 lb. box SAFEWAY CHOCOLATE BUTTERCREME BASE, MDM # 10201865, Distributed by Safeway Inc. PO Box 99 Pleasanton, CA 94566-0009
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·20078·2020-02-26

    Safavieh Recalls Aura and Silas Chests Due to Tip-Over Hazards

    Safavieh is recalling Aura and Silas 3-drawer chests because they can tip over or entrap children if not anchored to the wall.

    Product
    Aura and Silas 3-Drawer Chests
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1264-2020·2020-02-26

    Recall of Covidien Endo GIA Ultra Universal Staplers Due to Sterility Risk

    COVIDIEN LLC is recalling 2,180 units of Endo GIA Ultra Universal Staplers because the sterile barrier may be compromised, increasing the risk of infection.

    Product
    Covidien Endo GIA Ultra Universal Stapler 12 mm-intended for resection, transection in general surgery Item Code: EGIAUSTND
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1314-2020·2020-02-26

    Nobel Biocare Dense Bone Drill Recall Due to Sterility Concerns

    Nobel Biocare is recalling Dense Bone Drills because a packaging sealing issue may compromise sterility during shelf life.

    Product
    Dense Bone Drill NP 3.5x16 mm Single-Pat - Product Usage: Drills are intended to be used in the upper and lower jaw bone to prepare osteotomy prior to implant placement.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0723-2020·2020-02-26

    CSM Bakery Products Recalls Donut Icing Due to Plastic Polymer Contamination

    CSM Bakery Products is recalling 43 lb. pails of Glossy White Icing distributed by Krispy Kreme because pieces of plastic polymer were introduced into the sugar system.

    Product
    43 lb. pail GLOSSY WHITE ICING (1102507) donut icing, MDM # 10199098, Distributed by Krispy Kreme Doughnut Corporation 1814 Ivy Avenue, Winston-Salem, NC 27105
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1235-2020·2020-02-26

    Cardinal Health Recalls Presource Procedure Packs with Potential Sterility Issues

    Cardinal Health is recalling Presource Procedure Packs containing AAMI Level 3 surgical gowns because they may not be sterile due to improper environmental conditions during manufacturing.

    Product
    Presource Procedure Packs containing AAMI Level 3 surgical gowns, Multiple Catalog Numbers Produced Between September 1, 2018 and January 15, 2020. Additional kits produced through February 19, 2020 were included.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1315-2020·2020-02-26

    Nobel Biocare Dense Bone Drills Recalled for Sterility Concerns

    Nobel Biocare is recalling Dense Bone Drills because a packaging defect may compromise sterility during shelf life.

    Product
    Dense Bone Drill WP 5x13 mm Single-Pat - Product Usage: Drills are intended to be used in the upper and lower jaw bone to prepare osteotomy prior to implant placement.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V111000·2020-02-26

    Custom Fire Recalls 2017 Side Mount Pumper for Foam Pump Overheating

    Custom Fire is recalling one 2017 Side Mount Pumper because the foam pump system can overheat and fail, making firefighting foam unavailable.

    Product
    CUSTOM FIRE — CUSTOM FIRE SIDE MOUNT PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1332-2020·2020-02-26

    Siemens Luminos Agile Max X-ray System Recalled for Collision Risk

    Siemens is recalling 475 Luminos Agile Max X-ray systems because a bypass key can override collision controls, creating a risk of collision with obstacles or persons.

    Product
    Luminos Agile Max, Model No. 10762472 - Product Usage: Luminos Agile Max is a device intended to visualize anatomical structures by converting an X-ray pattern into a visible image. The system has medical applications ranging from gastrointestinal examinations to cranial…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1319-2020·2020-02-26

    Nobel Biocare Recalls Implant Retrieval Instruments Due to Sterility Concerns

    Nobel Biocare is recalling 423 implant retrieval instruments because a packaging defect may compromise sterility during shelf life.

    Product
    Implant Retrieval Instrument CC NP & Ext Hex WP 22 mm - Product Usage: They can be used to remove implants, if the implant connection has been damaged. It can be used to remove implants with internal conical connection, internal tri-channel connection or external hex connection.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1329-2020·2020-02-26

    Philips CombiDiagnost PCF X-ray System Software Recall

    Philips is recalling 131 CombiDiagnost PCF X-ray systems due to a software error that locks the table and an incorrectly installed thermos switch.

    Product
    CombiDiagnost PCF, Software v. 1.0.5, Product Code 709030 - Product Usage: Xray system, diagnostic, fluoroscopic, general purpose.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1282-2020·2020-02-26

    FDA Recalls Polysorb Sutures Due to Packaging Integrity Issues

    The FDA is recalling specific lots of Polysorb Braided Absorbable Sutures due to potential packaging integrity issues that may compromise sterility.

    Product
    Polysorb Braided Absorbable Suture 1 36 VIOLET GS-24, Item Code CL915 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1337-2020·2020-02-26

    Siemens Luminos dRF Max Recalled for Software Bug Affecting Patient Images

    Siemens Medical Solutions USA, Inc. is recalling 46 Luminos dRF Max digital radiography systems due to a software bug that may assign one image to two different patients, potentially affecting medical diagnosis.

    Product
    Luminos dRF Max, model no. 10762471 - Product Usage: Luminos dRF Max is a device intended to visualize anatomical structures by converting an X-ray pattern into a visible image. The system has medical applications ranging from gastrointestinal examinations to cranial, skeletal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1311-2020·2020-02-26

    Nobel Biocare Dental Drills Recalled Due to Packaging Seal Defects

    Nobel Biocare is recalling 264 tapered dental drills because a packaging sealing defect may compromise sterility during shelf life.

    Product
    Drill Tapered WP 5x10 mm Single-Pat - Product Usage: Drills are intended to be used in the upper and lower jaw bone to prepare osteotomy prior to implant placement.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0725-2020·2020-02-26

    CSM Bakery Products Recalls Simplicious Cream Cheese Icing Due to Plastic Contamination

    CSM Bakery Products is recalling 18 lb. pails of Simplicious Cream Cheese Icing because pieces of plastic polymer were introduced into the sugar system.

    Product
    18 lb. pail SIMPLICIOUS CREAM CHEESE ICING 18#PL, MDM # 10202840, Manufactured by Brill Inc. Tucker, GA 30084 1 866 982 7455 OR BRILLINC.COM
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·20V113000·2020-02-26

    Thomas Built Buses Saf-T-Liner C2 Recall for Exterior Light Failure

    Daimler Trucks North America is recalling 2017-2020 Thomas Built Buses Saf-T-Liner C2 school buses because the exterior warning lights and stop sign may fail, increasing injury risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0729-2020·2020-02-26

    CSM Bakery Products Recalls Donut Icing Due to Plastic Polymer Contamination

    CSM Bakery Products is recalling 43 lb. pails of White 'n Glossy Icing donut icing because pieces of plastic polymer were introduced into the sugar system.

    Product
    43 lb. pail WHITE 'N GLOSSY ICING donut icing, MDM # 10203280, Manufactured by Brill Inc. Tucker, GA 30084 1 866 982 7455 OR BRILLINC.COM
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1233-2020·2020-02-26

    Siemens Dimension Vista Enzymatic Creatinine Reagent Recalled for Interference

    Siemens Healthcare Diagnostics is recalling Dimension Vista Enzymatic Creatinine reagent because it may produce falsely depressed results for patients taking phenindione.

    Product
    Dimension Vista Enzymatic Creatinine (ECREA) reagent, SMN 10700444
    Category
    Medical Device
    Distribution
    Distributed nationwide