FDA Adverse Event Malfunction Summary report: N

WAND 900-115 15MM DISPOSABLE

MDR report key: 6099294 · Received November 14, 2016

Report

Report Number
1226420-2016-00181
Event Type
Malfunction
Date Received
November 14, 2016
Date of Event
October 20, 2016
Report Date
October 20, 2016
Manufacturer
MEDTRONIC ADVANCED ENERGY, LLC
Product Code
GEI
PMA / PMN Number
K152596
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
KY, US
Reporter Occupation
HEALTH PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

PRODUCT EVENT: 701519485 RECEIPT OF COMPLAINT INFORMATION TRIGGERED FORMAL INVESTIGATION PR 325854 WHICH IS CURRENTLY IN PROCESS. A GOOD FAITH EFFORT WILL BE MADE TO OBTAIN THE APPLICABLE INFORMATION RELEVANT TO THE REPORT. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Additional Manufacturer Narrative · 1

(B)(4). A GOOD FAITH EFFORT WILL BE MADE TO OBTAIN THE APPLICABLE INFORMATION RELEVANT TO THE REPORT. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Additional Manufacturer Narrative · 1

IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Description of Event or Problem · 1

DURING A BREAST ONCOLOGY CASE, ONE OF THE WIRES BROKE DURING CAPTURE ON THE INTACT WAND. THE WIRE REMAINED ATTACHED TO THE DEVICE TIP. NOTHING REMAINED IN THE PATIENT AND THERE WAS NO PATIENT HARM.

Description of Event or Problem · 1

DURING A BREAST ONCOLOGY CASE, ONE OF THE WIRES BROKE DURING CAPTURE ON THE INTACT WAND. THE WIRE REMAINED ATTACHED TO THE DEVICE TIP. NOTHING REMAINED IN THE PATIENT AND THERE WAS NO PATIENT HARM.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
749855 WAND 900-115 15MM DISPOSABLE ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES GEI MEDTRONIC ADVANCED ENERGY, LLC 900-115 E37153

Patients

Seq Age Sex Outcome Treatment
1 67 YR