FDA Adverse Event Injury Summary report: N

5.0 CM SHORT ATTACHMENT

MDR report key: 3140732 · Received May 31, 2013

Report

Report Number
1045834-2013-02235
Event Type
Injury
Date Received
May 31, 2013
Date of Event
March 13, 2013
Report Date
March 20, 2013
Manufacturer
DEPUY SYNTHES POWER TOOLS
Product Code
HBC
PMA / PMN Number
K011444
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SZ
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE DEVICE HAS BEEN RETURNED AND IS CURRENTLY UNDERGOING EVALUATION. ONCE THE EVALUATION HAS BEEN COMPLETED OR IF ADDITIONAL INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SENT. (B)(4).

Additional Manufacturer Narrative · 1

DEVICE EVALUATION: THE ACTUAL DEVICE WAS RECEIVED FOR EVALUATION. RELIABILITY ENGINEERING EVALUATED THE DEVICE. FUNCTIONAL TESTING REVEALED THAT THE DEVICE GOT HOT IMMEDIATELY. A VISUAL INSPECTION REVEALED THAT THE BEARINGS WERE HIGHLY CORRODED. THEREFORE, THE REPORTED CONDITION WAS DUPLICATED AND CONFIRMED. EVIDENCE INDICATES THIS WAS DUE TO IMPROPER CLEANING. IF ADDITIONAL INFORMATION SHOULD BECOME AVAILABLE, A SUPPLEMENTAL MEDWATCH REPORT WILL BE SENT ACCORDINGLY. (B)(4).

Description of Event or Problem · 1

A REPORT FROM (B)(6) WAS RECEIVED STATING THAT THERE WAS AN INCIDENT OF THE ATTACHMENT DEVICE OVERHEATING, AND CONSEQUENTLY BURNING THROUGH TWO SETS OF THE SURGEON'S GLOVES. AS A RESULT, THERE WAS A SUPERFICIAL BURN (RED MARK) ON THE SURGEON'S HAND. NO MEDICAL INTERVENTION WAS REPORTED OR REQUIRED FOR THE SURGEON¿S SUPERFICIAL BURN. ALLEGEDLY, THE BURR CAUSED THE SURGEON'S INJURY. THE SURGICAL PROCEDURE BEING PERFORMED AT THAT TIME WAS A CRANIOTOMY RESECTION OF A TUMOR. THERE WAS NO INJURY TO THE PATIENT AND NO MEDICAL INTERVENTION WAS REQUIRED. THERE WAS NO DELAY IN SURGERY REPORTED. ALLEGEDLY, THE DRILL STOPPED IMMEDIATELY AND THE SURGEON CHANGED THE BURNED GLOVES AND REPLACED THEM WITH TWO NEW SETS OF SURGICAL GLOVES. THE SURGERY WAS COMPLETED SUCCESSFULLY WITH AN ALTERNATE DEVICE. REPORTEDLY, THE PHYSICIAN WAS CONCERNED THAT THE HEAT BUILD UP WAS ¿VERY QUICK AND SUDDEN." NO FURTHER INFORMATION IS AVAILABLE. IF ANY FURTHER INFORMATION SHOULD BECOME AVAILABLE. THIS NOTIFICATION WILL BE UPDATED ACCORDINGLY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
241939 5.0 CM SHORT ATTACHMENT MOTOR, DRILL, ELECTRIC - ATTACHMENT HBC DEPUY SYNTHES POWER TOOLS

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention EMAX 2 PLUS MOTOR, S-4B BURR