The Recall Desk

State

Northern Mariana Islands product recalls

73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

32651–32675 of 73745

  • ModerateFDA (Devices)·Z-2205-2019·2019-08-14

    Philips Azurion X-ray systems recalled for cold restart delays

    Philips is recalling Azurion interventional fluoroscopic X-ray systems because a cold restart may take up to 7 minutes, potentially delaying treatment.

    Product
    Philips Azurion systems with software version R1.2 -Interventional Fluoroscopic X-ray system as follows: Azurion 3 M12, Azurion 3 M15, Azurion 7 B12, Azurion 7 B20, Azurion 7 M12, Azurion 7 M20 Models: 722063, 722064, 722067, 722068, 722078, 722079. Product Usage: The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1633-2019·2019-08-14

    CVS Children's Nasal Saline Drops Recalled for B. cepacia Contamination Risk

    Unipharma, LLC is recalling CVS Health Children's Nasal Saline Drops due to a precautionary measure regarding potential contamination with B. cepacia bacteria.

    Product
    CVS Health Children's Nasal Saline Drops with Himalayan Salt Saline Nasal Moisturizer, 30 single-use vials per Carton,0.05 fl. oz. (1.5 mL) each 1.5 fl. oz. (45 mL) total, Distributed by: CVS Pharmacy, Inc. One CVS Drive Woonsocket, RI 02895, UPC 050428598207
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2217-2019·2019-08-14

    MedComp Recalls Hemodialysis Catheter Kits Due to Labeling Error

    Medical Components, Inc. is recalling 6,830 hemodialysis catheter insertion kits because the tray labels incorrectly identify the included introducer as valved.

    Product
    14F x 30CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits, Item No. MC061425 Product Usage: An aid for introducing a hemodialysis catheter
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2174-2019·2019-08-14

    Ortho VITROS 250 Chemistry System Recalled for Software Calibration Anomaly

    Ortho Clinical Diagnostics is recalling 30 VITROS 250 Chemistry Systems due to a software anomaly that may cause unsuccessful calibrations.

    Product
    VITROS 250 Chemistry System, clinical chemistry analyzer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1610-2019·2019-08-14

    Herbal Doctor Remedies Recalls Migraine Off Capsules for Manufacturing Deviations

    Herbal Doctor Remedies is recalling Migraine Off Capsules because they were manufactured outside of required Good Manufacturing Practices controls.

    Product
    Migraine Off Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1592-2019·2019-08-14

    Herbal Doctor Remedies Recalls Cardia Forte Capsules for CGMP Deviations

    Herbal Doctor Remedies is recalling Cardia Forte 500 mg capsules because they were manufactured outside of current Good Manufacturing Practices controls.

    Product
    Cardia Forte, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1626-2019·2019-08-14

    Herbal Doctor Remedies Recalls Appetrol Capsules for CGMP Deviations

    Herbal Doctor Remedies is recalling Appetrol Capsules because they were manufactured outside of current Good Manufacturing Practice controls.

    Product
    Appetrol Capsules, Distributed by Herbal Doctor Remedies, Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2146-2019·2019-08-14

    Geistlich Bio-Oss Pen Recalled Due to Visible Plastic Debris

    Geistlich Pharma is recalling Bio-Oss Pen units because visible green plastic debris was found on the outer barrel when unscrewing the cap.

    Product
    Geistlich Bio-Oss Pen, Sterile cancellous granules in an applicator, 0.25-1.mm 0.5g, For single use only, Part Number 20116 - Product Usage: Augmentation or reconstructive treatment of the alveolar ridge; Filling of infrabony periodontal defects; Filling of defects after root…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1620-2019·2019-08-14

    Herbal Doctor Remedies Recalls Worm Off Capsules Due to Manufacturing Deviations

    Herbal Doctor Remedies is recalling Worm Off 500 mg capsules because they were manufactured outside of required Good Manufacturing Practices controls.

    Product
    Worm Off, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2170-2019·2019-08-14

    Centurion Driveline Management System 1 Daily Kit Recalled for Packaging Risk

    Centurion Medical Products is recalling 6,180 Driveline Management System 1 Daily Kits because sterile packaging may be compromised.

    Product
    DRIVELINE MANAGEMENT SYSTEM 1 DAILY Kit Code: DT18440A - Product Usage: Kit is used for Driveline Maintenance and Securement of Line for general patient population.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2147-2019·2019-08-14

    Geistlich Bio-Oss Pen Recalled Due to Visible Plastic Debris

    Geistlich Pharma North America is recalling Bio-Oss Pen applicators because a visible piece of green plastic was found on the outer barrel when unscrewing the cap.

    Product
    Geistlich Bio-Oss Pen, Sterile cancellous granules in an applicator, 1-2mm 0.5g, For single use only, Part Number 20126 - Product Usage: Augmentation or reconstructive treatment of the alveolar ridge; Filling of infrabony periodontal defects; Filling of defects after root…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1590-2019·2019-08-14

    Herbal Doctor Remedies Recalls Baby Saver Capsules for Manufacturing Deviations

    Herbal Doctor Remedies is recalling Baby Saver Capsules because they were manufactured outside of required Good Manufacturing Practices controls.

    Product
    Baby Saver Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1607-2019·2019-08-14

    Herbal Doctor Remedies Recalls Lung Fixer Capsules for Manufacturing Deviations

    Herbal Doctor Remedies is recalling Lung Fixer Capsules because they were manufactured outside of required Good Manufacturing Practices controls.

    Product
    Lung Fixer Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2186-2019·2019-08-14

    Philips Ingenuity CT Recalled for Potential Cardiac Image Labeling Error

    Philips is recalling 92 Ingenuity CT systems because cardiac images may be incorrectly labeled as having phase tolerance applied when it was not.

    Product
    Ingenuity CT, Model # 728326, computed tomography x-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1617-2019·2019-08-14

    Herbal Doctor Remedies Recalls Stone Purger Capsules for Manufacturing Deviations

    Herbal Doctor Remedies is recalling Stone Purger Capsules because they were manufactured outside of required Good Manufacturing Practices controls.

    Product
    Stone Purger Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1618-2019·2019-08-14

    Herbal Doctor Remedies Recalls Thyro-H Capsules for Manufacturing Violations

    Herbal Doctor Remedies is recalling Thyro-H 500 mg capsules because they were manufactured outside of current Good Manufacturing Practices controls.

    Product
    Thyro-H, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2182-2019·2019-08-14

    Ortho VITROS 4600 Chemistry System Recalled for Software Calibration Anomaly

    Ortho Clinical Diagnostics is recalling nine VITROS 4600 Chemistry Systems due to a software anomaly that may cause unsuccessful calibration.

    Product
    VITROS 4600 Chemistry System, clinical chemistry analyzer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2144-2019·2019-08-14

    Biomet 3i Recalls Titanium Abutments Due to Manufacturing Defect

    Biomet 3i is recalling 49 units of Certain Bellatek Titanium Abutments because a manufacturing defect prevents the screw from seating correctly.

    Product
    CERTAIN(R) BELLATEK(R) TITANIUM ABUTMENT 3.4MM, Item Number ILDAT3 - Product Usage:BIOMET3i Restorative products are intended for use as an accessory to endosseous dental implants for placement in the maxilla and mandible
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1619-2019·2019-08-14

    Herbal Doctor Remedies Recalls Vertigo Off Capsules for Manufacturing Deviations

    Herbal Doctor Remedies is recalling Vertigo Off Capsules because they were manufactured outside of required Good Manufacturing Practices controls.

    Product
    Vertigo Off Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1603-2019·2019-08-14

    Herbal Doctor Remedies Recalls Herpes-V Balm for Manufacturing Violations

    Herbal Doctor Remedies is recalling Herpes-V Balm because it was manufactured outside of required Good Manufacturing Practices controls.

    Product
    Herpes-V Balm, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2190-2019·2019-08-14

    Philips iCT SP Computed Tomography Systems Recalled for Image Labeling Error

    Philips is recalling 27 iCT SP computed tomography systems because images may be incorrectly labeled as having phase tolerance applied when it was not.

    Product
    iCT SP Model # 728311, computed tomography x-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1601-2019·2019-08-14

    Herbal Doctor Remedies Recalls Herpes-P Capsules for Manufacturing Deviations

    Herbal Doctor Remedies is recalling Herpes-P 500 mg capsules because they were manufactured outside of current Good Manufacturing Practices controls.

    Product
    Herpes-P, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2184-2019·2019-08-14

    Ortho VITROS 5,1 FS Chemistry System Recalled for Software Calibration Issue

    Ortho Clinical Diagnostics is recalling 55 VITROS 5,1 FS Chemistry Systems due to a software anomaly that may cause unsuccessful calibrations.

    Product
    VITROS 5,1 FS Chemistry System, clinical chemistry analyzer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2100-2019·2019-08-14

    ASTRA Lidar System Recalled for Incorrect Class 1 Laser Labeling

    ASTRA, LLC is recalling one Lidar System for Erosion Flume Application due to incorrect labeling of a Class 1 laser product.

    Product
    Lidar System for Erosion Flume Application Class 1 Laser Product Product Usage: Product is installed and fixed above a dynamic indoor flume designed for modeling water erosion in an indoor research environment with limited human access
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1595-2019·2019-08-14

    Dragon Pain Oil Recalled for Manufacturing Process Deviations

    Herbal Doctor Remedies is recalling Dragon Pain Oil because it was manufactured outside of required Good Manufacturing Practices controls.

    Product
    Dragon Pain Oil, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide