FDA Adverse Event Malfunction Summary report: N

5.0 CM SHORT ATTACHMENT

MDR report key: 3962872 · Received June 11, 2014

Report

Report Number
1045834-2013-16448
Event Type
Malfunction
Date Received
June 11, 2014
Date of Event
October 5, 2011
Report Date
October 5, 2011
Manufacturer
DEPUY SYNTHES POWER TOOLS
Product Code
HBC
PMA / PMN Number
K011444
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IT
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

THE DEVICE WAS RECEIVED BY DEPUY SYNTHES POWER TOOLS. THE DEVICE WAS EVALUATED, AND DURING SERVICE THE DEVICE FAILED THE CUTTER INSERTION TEST. IF ADDITIONAL INFORMATION BECOMES AVAILABLE A SUPPLEMENTAL REPORT WILL BE SUBMITTED. REF: (B)(4).

Description of Event or Problem · 1

REPORT RECEIVED FROM (B)(6) STATING THAT SERVICE WAS REQUIRED FOR THE DEVICE. DURING SERVICE THE INABILITY TO INSERT THE CUTTER WAS NOTED. THE DEVICE WAS NOT BEING USED IN SURGERY. IT IS UNKNOWN IF INJURY OR MEDICAL INTERVENTION OCCURRED. THERE WAS NO ADDITIONAL INFORMATION PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
345476 5.0 CM SHORT ATTACHMENT SURGICAL DRILL ATTACHMENT HBC DEPUY SYNTHES POWER TOOLS

Patients

Seq Age Sex Outcome Treatment
1