FDA Adverse Event Malfunction Summary report: N

11.0 CM LONG ATTACHMENT

MDR report key: 3973784 · Received June 17, 2014

Report

Report Number
1045834-2013-16476
Event Type
Malfunction
Date Received
June 17, 2014
Date of Event
June 18, 2012
Report Date
June 18, 2012
Manufacturer
DEPUY SYNTHES POWER TOOLS
Product Code
HBC
PMA / PMN Number
K011444
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MO, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

THE DEVICE WAS RECEIVED BY DEPUY SYNTHES POWER TOOLS. THE DEVICE WAS EVALUATED AND THE ISSUE OF CANNOT INSERT CUTTER WAS FOUND. THE DEVICE FAILED PRE-REPAIR DIAGNOSTIC ASSESSMENT CUTTER INSERTION VERIFICATION. IF ADDITIONAL INFORMATION IS RECEIVED A SUPPLEMENTAL REPORT WILL BE SUBMITTED. REF: (B)(4).

Description of Event or Problem · 1

REPORT RECEIVED FROM THE USA STATING THAT SERVICE WAS REQUIRED FOR THE DEVICE. DURING SERVICE, THE ISSUE OF CANNOT INSERT CUTTER WAS FOUND. IT IS UNKNOWN IF THE DEVICE WAS BEING USED DURING SURGERY. IT IS UNKNOWN IF INJURY OR MEDICAL INTERVENTION OCCURRED. NO ADDITIONAL INFORMATION WAS PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
355129 11.0 CM LONG ATTACHMENT SURGICAL DRILL ATTACHMENT HBC DEPUY SYNTHES POWER TOOLS

Patients

Seq Age Sex Outcome Treatment
1