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.

32601–32625 of 73745

  • HighFDA (Devices)·Z-2210-2019·2019-08-14

    Bard EnCor Breast Biopsy Probes Recalled for Leaks and Suction Issues

    Bard Peripheral Vascular Inc is recalling EnCor Breast Biopsy Probes due to increased complaints of leaks, suction issues, and failure to obtain tissue samples.

    Product
    EnCor Breast Biopsy Probes, packaged individually in sterile pouches, 5 pouches/carton, single use, Rx, catalog/REF numbers 10GV Upright (Vertical) - REF ECP0110GV. Product Usage: Indicated for use in acquiring tissue for diagnosing breast abnormalities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1636-2019·2019-08-14

    RXQ Compounding Recalls Ascorbic Acid Injection Due to Crystallization

    RXQ Compounding LLC is voluntarily recalling Ascorbic Acid 500 MG/ML Injection due to crystallization. The recall covers all lots within expiry distributed nationwide.

    Product
    Ascorbic Acid 500 MG/ML (Non-Corn) INJ (MDV), 50 mL per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0975-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2180-2019·2019-08-14

    Ortho VITROS 5600 Analyzer Recalled for Software Calibration Anomaly

    Ortho Clinical Diagnostics is recalling 89 VITROS 5600 clinical chemistry analyzers worldwide due to a software anomaly that may cause unsuccessful calibrations.

    Product
    VITROS 5600 Integrated System, clinical chemistry analyzer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2187-2019·2019-08-14

    Philips CT System Recall for Incorrect Cardiac Image Labeling

    Philips is recalling 116 CT systems because cardiac images may be incorrectly labeled as having phase tolerance applied when it was not.

    Product
    Ingenuity Core128 Model # 728323, computed tomography x-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1611-2019·2019-08-14

    Herbal Doctor Remedies Recalls Pain Away Capsules for Manufacturing Deviations

    Herbal Doctor Remedies is recalling Pain Away 500 mg capsules because they were manufactured outside of required Good Manufacturing Practices.

    Product
    Pain Away, 500 mg Capsules, 90-count bottles, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1605-2019·2019-08-14

    Herbal Doctor Remedies Recalls Lube Lax Capsules for Manufacturing Violations

    Herbal Doctor Remedies is recalling Lube Lax Capsules because they were manufactured outside of current Good Manufacturing Practices controls.

    Product
    Lube Lax Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1614-2019·2019-08-14

    Herbal Doctor Remedies Recalls Psoriasis Balm Due to Manufacturing Deviations

    Herbal Doctor Remedies is recalling Psoriasis Balm because it was manufactured outside of current Good Manufacturing Practice controls.

    Product
    Psoriasis Balm, 60 gram, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1597-2019·2019-08-14

    Herbal Doctor Remedies Recalls Fungo Balm Due to Manufacturing Deviations

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

    Product
    Fungo Balm, 30 gram, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1594-2019·2019-08-14

    Dragon Pain Balm Recalled for CGMP Manufacturing Deviations

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

    Product
    Dragon Pain Balm, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1632-2019·2019-08-14

    Unipharma Recalls DrKids Children's Allergy Relief Diphenhydramine Due to B. cepacia Risk

    Unipharma is recalling DrKids Children's Allergy Relief Diphenhydramine vials due to a precautionary measure regarding potential contamination with B. cepacia bacteria.

    Product
    DrKids Children's Allergy Relief Diphenhydramine HCl 12.5 mg/5 mL Antihistamine, Mixed berry Flavor, 20 Pre-measured Single-Use vials per Carton, Manufactured in USA by: Unipharma, LLC. Tamarac, FL 33321, UPC 370302255010
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2143-2019·2019-08-14

    Biomet 3i Recalls Certain Bellatek Tin Abutments Due to Manufacturing Defect

    Biomet 3i is recalling 2 units of Bellatek Tin Abutments because a manufacturing defect causes the screw head to seat too deep without a positive stop.

    Product
    CERTAIN(R) BELLATEK(R) TIN ABUTMENT 3.4MM, Item Number ILDAN3 - 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-1623-2019·2019-08-14

    Herbal Doctor Remedies Recalls Smoke End Capsules for Manufacturing Violations

    Herbal Doctor Remedies is recalling Smoke End Capsules because they were manufactured outside of current Good Manufacturing Practices controls.

    Product
    Smoke End Capsules,Distributed Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1615-2019·2019-08-14

    Herbal Doctor Remedies Recalls Sperm Booster for Manufacturing Violations

    Herbal Doctor Remedies is recalling Sperm Booster because it was manufactured outside of required Good Manufacturing Practice controls.

    Product
    Sperm Booster, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1600-2019·2019-08-14

    Herbal Doctor Remedies Recalls Herpes-G Capsules for Manufacturing Violations

    Herbal Doctor Remedies is recalling Herpes-G Capsules because they were manufactured outside of current Good Manufacturing Practices (CGMP) controls.

    Product
    Herpes-G Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2175-2019·2019-08-14

    Ortho VITROS 250 Chemistry System Recalled for Software Calibration Anomaly

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

    Product
    VITROS 250 Chemistry System, clinical chemistry analyzer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2216-2019·2019-08-14

    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 describe the included introducer as valved.

    Product
    14F x 24CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits, Item No. MC061424 Product Usage: An aid for introducing a hemodialysis catheter
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2178-2019·2019-08-14

    Ortho VITROS Calibrator Kit 32 Recalled for Software Anomaly

    Ortho Clinical Diagnostics is recalling VITROS Chemistry Products Calibrator Kit 32 due to a software anomaly that may cause unsuccessful calibration.

    Product
    VITROS Chemistry Products Calibrator Kit 32, for use with VITROS clinical chemistry analyzer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1602-2019·2019-08-14

    Herbal Doctor Remedies Recalls Herpes-S Capsules Due to Manufacturing Deviations

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

    Product
    Herpes-S, 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-1612-2019·2019-08-14

    Herbal Doctor Remedies Recalls Pain Stopper Capsules for Manufacturing Deviations

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

    Product
    Pain Stopper, 500 mg Capsules, 90-count bottles, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1621-2019·2019-08-14

    Herbal Doctor Remedies Recalls Yeast Douche Powder for Manufacturing Deviations

    Herbal Doctor Remedies is recalling Yeast Douche Powder because it was manufactured outside of required Good Manufacturing Practices controls.

    Product
    Yeast Douche Powder, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1622-2019·2019-08-14

    Herbal Doctor Remedies Recalls Detensin Capsules Due to Manufacturing Deviations

    Herbal Doctor Remedies is recalling Detensin 500 mg capsules because they were manufactured outside of current Good Manufacturing Practice controls.

    Product
    Detensin, 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-1588-2019·2019-08-14

    Herbal Doctor Remedies Recalls Asthma Balm Due to Manufacturing Deviations

    Herbal Doctor Remedies is recalling Asthma Balm 60 gram because it was manufactured outside of current Good Manufacturing Practices controls.

    Product
    Asthma Balm 60 gram, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2191-2019·2019-08-14

    Philips Brilliance 64 CT System Recalled for Image Labeling Error

    Philips is recalling 582 Brilliance 64 CT systems because images may be incorrectly labeled as having phase tolerance applied when it was not.

    Product
    Brilliance 64 Model # 728231, computed tomography x-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2215-2019·2019-08-14

    MedComp Recalls Hemodialysis Catheter Kits Due to Introducer Mismatch

    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 20CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits, Item No. MC061423 Product Usage: An aid for introducing a hemodialysis catheter
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2193-2019·2019-08-14

    Philips Ingenuity TF PET/CT Recalled for Cardiac Image Labeling Error

    Philips is recalling 12 Ingenuity TF PET/CT systems because cardiac images may be incorrectly labeled as having phase tolerance applied when it was not.

    Product
    Ingenuity TF PET/CT Model # 882456, computed tomography x-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide