FDA Adverse Event Malfunction Summary report: N

ANSPACH® XMAX

MDR report key: 4170654 · Received October 14, 2014

Report

Report Number
1045834-2014-14027
Event Type
Malfunction
Date Received
October 14, 2014
Report Date
February 5, 2013
Manufacturer
DEPUY SYNTHES POWER TOOLS
Product Code
ERL
PMA / PMN Number
PK131053
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SF
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

DURING PRE-REPAIR ASSESSMENT PERFORMED BY TECHNICIAN, IT WAS NOTED THAT THE LOCKING COMPONENTS WERE DAMAGED. DEVICE WAS INSPECTED AND REPAIRED.

Description of Event or Problem · 1

CUSTOMER REPORTED DRILL LOSES POWER. THIS IS REPORT 1 OF 1 FOR EVENT #COM-(B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
651488 ANSPACH® XMAX DRILL, SURGICAL, ENT (ELECTRIC OR PNEUMATIC) INCLUDING HANDPIECE ERL DEPUY SYNTHES POWER TOOLS

Patients

Seq Age Sex Outcome Treatment
1