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Nester G52752Recalls & reported problems

Cook Incorporated · Nester Embolization Coil · Class 2 · Implant

All models of Nester (38)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
3
Deaths reported
0
Injuries reported
3
Recalls naming it
0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00827002527522), received between Jan 18, 2021 and Jan 18, 2021 — classified as 3 injuries.

The most frequently reported specific device problem is “Migration” (3 reports).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Migration3

Patient problems

  • Patient Problem/Medical Problem3

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

  • InjuryJan 18, 2021Migration; Migration

    NO ADDITIONAL INFORMATION REGARDING THE PATIENT AND/OR EVENT HAS BEEN RECEIVED SINCE THE PREVIOUS MEDWATCH REPORT WAS SENT.

    Patient problems: Patient Problem/Medical Problem

    MAUDE report 11187046 ↗
  • InjuryJan 18, 2021Migration; Migration

    IT WAS REPORTED BY A LAW FIRM "IN 2016, (PATIENT) SUFFERED FROM VARICOSE VEINS OF THE LOWER EXTREMITIES AND PELVIC CONGESTION SYNDROME." PATIENT ELECTED TO HAVE AN EMBOLIZATION PROCEDURE, DURING WHICH SEVERAL COOK NESTER AND TORNADO EMBOLIZATION COILS WERE IMPLANTED. REPORT STATES THE PATIENT "EXPERIENCED A LITANY OF HEALTH ISSUES UNTIL SHE HAD THE COILS REMOVED, INCLUDING: EXTREME PAIN; AUTOIMMUNE DIAGNOSES; DIFFICULTY WALKING; AND RENAL ISSUES. ON OR ABOUT (B)(6) 2018, PATIENT OPTED TO HAVE THE COILS REMOVED, AT WHICH TIME IT WAS FOUND THE COILS HAD PERFORATED AND MIGRATED. REPORT FURTHER STATES "AFTER THE COILS WERE REMOVED, PATIENT BEGAN TO FEEL RELIEF." MEDICAL RECORDS INDICATED THE FOLLOWING: ON (B)(6) 2016, PATIENT UNDERWENT BILATERAL COILING OF GONADAL VEINS DUE TO REFLUX AND DILATION. BILATERAL OVARIAN VEIN INSUFFICIENCY WITH MARKEDLY ENLARGED OVARIAN VEINS AND PELVIC VARICES WAS CONFIRMED. SUCCESSFUL BILATERAL OVARIAN VEIN COIL EMBOLIZATION DISTAL TO PROXIMAL WAS PERFORMED AND PERIODIC VENOGRAMS CONFIRMED STASIS AND CLOSURE OF OVARIAN VEIN BRANCHES. THERE WERE NO IMMEDIATE COMPLICATIONS AND UPON REMOVAL OF THE CATHETER AND SHEATH, HEMOSTASIS WAS ACHIEVED WITH MANUAL PRESS

    Patient problems: Patient Problem/Medical Problem

    MAUDE report 11187043 ↗
  • InjuryJan 18, 2021Migration; Migration

    IT WAS REPORTED BY A LAW FIRM "IN 2016, (PATIENT) SUFFERED FROM VARICOSE VEINS OF THE LOWER EXTREMITIES AND PELVIC CONGESTION SYNDROME." PATIENT ELECTED TO HAVE AN EMBOLIZATION PROCEDURE, DURING WHICH SEVERAL COOK NESTER AND TORNADO EMBOLIZATION COILS WERE IMPLANTED. REPORT STATES THE PATIENT "EXPERIENCED A LITANY OF HEALTH ISSUES UNTIL SHE HAD THE COILS REMOVED, INCLUDING: EXTREME PAIN; AUTOIMMUNE DIAGNOSES; DIFFICULTY WALKING; AND RENAL ISSUES. ON OR ABOUT (B)(6) 2018, PATIENT OPTED TO HAVE THE COILS REMOVED, AT WHICH TIME IT WAS FOUND THE COILS HAD PERFORATED AND MIGRATED. REPORT FURTHER STATES "AFTER THE COILS WERE REMOVED, PATIENT BEGAN TO FEEL RELIEF." MEDICAL RECORDS INDICATED THE FOLLOWING: ON (B)(6) 2016, PATIENT UNDERWENT BILATERAL COILING OF GONADAL VEINS DUE TO REFLUX AND DILATION. BILATERAL OVARIAN VEIN INSUFFICIENCY WITH MARKEDLY ENLARGED OVARIAN VEINS AND PELVIC VARICES WAS CONFIRMED. SUCCESSFUL BILATERAL OVARIAN VEIN COIL EMBOLIZATION DISTAL TO PROXIMAL WAS PERFORMED AND PERIODIC VENOGRAMS CONFIRMED STASIS AND CLOSURE OF OVARIAN VEIN BRANCHES. THERE WERE NO IMMEDIATE COMPLICATIONS AND UPON REMOVAL OF THE CATHETER AND SHEATH, HEMOSTASIS WAS ACHIEVED WITH MANUAL PRESS

    Patient problems: Patient Problem/Medical Problem

    MAUDE report 11187001 ↗

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