FDA Adverse Event Injury Summary report: N

LIGASURE PRECISE

MDR report key: 9207398 · Received October 18, 2019

Report

Report Number
1717344-2019-01369
Event Type
Injury
Date Received
October 18, 2019
Date of Event
February 22, 2016
Report Date
October 18, 2019
Manufacturer
COVIDIEN MFG DC BOULDER
Product Code
GEI
UDI-DI
10884524001463
PMA / PMN Number
K010010
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GM
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

(B)(4). TITLE: IS SUTURELESS THYROID SURGERY SAFE IN THE HANDS OF SURGICAL TRAINEES. A SINGLE CENTRE RETROSPECTIVE STUDY SOURCE: AMBE AND WASSENBERG BMC RES NOTES (2016) 9:118 DOI 10.1186/S13104-016-1940-7. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Description of Event or Problem · 1

PLI 10: ACCORDING TO LITERATURE SOURCE OF STUDY PERFORMED FROM JANUARY 2011 UNTIL OCTOBER 2013, TWO HUNDRED AND EIGHT PATIENTS UNDERWENT THYROID SURGERY. SURGERY WAS PERFORMED IN 147 CASES (70.7 %) BY CONSULTANTS (CONSULTANT GROUP) AND IN 61 CASES (29.3 %) BY SURGICAL TRAINEES (TRAINEE GROUP). THE LIGASURE® PRECISE (COVIDIEN, BOULDER, CO, USA) WAS USED IN ALL CASES. THE RATE OF POSTOPERATIVE HEMORRHAGE WAS 3.4 % (7/208). AND THE INCIDENCE OF PERMANENT RECURRENT LARYNGEAL NERVE INJURY WAS 0.9 % (2 CASES).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1003766 LIGASURE PRECISE ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES GEI COVIDIEN MFG DC BOULDER LS1200 10884524001463

Patients

Seq Age Sex Outcome Treatment
1 58 YR Other