FDA Adverse Event Other Summary report: N

VC EVH, OD, SMR, VD, BP

MDR report key: 2303762 · Received October 7, 2011

Report

Report Number
1718850-2011-00128
Event Type
Other
Date Received
October 7, 2011
Date of Event
September 7, 2011
Report Date
September 8, 2011
Manufacturer
SORIN GROUP USA, INC.
Product Code
GEI
PMA / PMN Number
K102983
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

PATIENT INFORMATION WAS REQUESTED BUT NOT PROVIDED AT THIS TIME. SORIN GROUP (B)(4) RECEIVED A REPORT THAT THE TIP OF THE BIPOLAR DEVICE BROKE OFF IN THE PATIENT'S LEG DURING A VEIN HARVESTING PROCEDURE. THE TIP WAS RETRIEVED. THE FACILITY REPORTED THAT THE PATIENT WAS FINE. THERE WAS NO HARM TO THE PATIENT AS A RESULT OF THIS INCIDENT. THE FACILITY STATED THAT THE BIPOLAR DEVICE WAS NOT SAVED FOR EVALUATION. WITHOUT AN EVALUATION OF THE DEVICES INVOLVED, NO ROOT CAUSE FOR THE REPORTED FAILURE CAN BE DETERMINED. THE INSTRUCTIONS FOR USE STATE "TO ENSURE THAT THE INSTRUMENT WILL CLOSE PROPERLY, DO NOT INSERT TOO MUCH TISSUE IN THE JAWS", DO NOT ADVANCE OR TORQUE THE INSTRUMENT WITH THE JAWS OPEN OR USE THE JAWS FOR SPREAD DISSECTION. THESE ACTIONS WILL DAMAGE THE INSTRUMENT". NO FURTHER ACTION IS DEEMED NECESSARY AT THIS TIME.

Description of Event or Problem · 1

SORIN GROUP (B)(4) RECEIVED A REPORT THAT THE TIP OF THE BIPOLAR DEVICE BROKE OFF IN THE PATIENT'S LEG DURING A VEIN HARVESTING PROCEDURE. THE TIP WAS RETRIEVED. THERE WAS NO REPORT OF HARM TO THE PATIENT AS A RESULT OF THIS INCIDENT. IT WAS REPORTED THAT THE PATIENT IS FINE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 VC EVH, OD, SMR, VD, BP BIPOLAR DEVICE GEI SORIN GROUP USA, INC. NA 1117400005

Patients

Seq Age Sex Outcome Treatment
1