FDA Adverse Event Malfunction Summary report: N

LOW PRESS BLACK MAX HANDPIECE

MDR report key: 4182337 · Received October 17, 2014

Report

Report Number
1045834-2014-13887
Event Type
Malfunction
Date Received
October 17, 2014
Report Date
February 11, 2013
Manufacturer
DEPUY SYNTHES POWER TOOLS
Product Code
HBB
PMA / PMN Number
PK831756
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
UK
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

ADDITIONAL NARRATIVE: SYNTHES IS SUBMITTING THIS REPORT AS A RESULT OF REMEDIATION ACTIVITIES RELATED TO SYNTHES SERVICE AND REPAIR FILES LEGACY REVIEW/REMEDIATION PROTOCOL-COMPLAINT HANDLING AND MDR REPORTING. DEVICE LISTED IN THIS REPORT IS USED FOR TREATMENT, NOT DIAGNOSIS. ANY ADDITIONAL INFORMATION RECEIVED REGARDING THIS EVENT AFTER FILING THIS REPORT SHALL BE FILED ON A SUPPLEMENTAL MDR. DURING PRE-REPAIR ASSESSMENT PERFORMED BY A TECHNICIAN, FUNCTIONAL TESTING WAS PERFORMED AND REVEALED THE BEARING WAS WORN AND THE BLADE BROKEN. THIS WAS ATTRIBUTED TO NORMAL WEAR. THE BLADE WAS REPLACED. THE DEVICE WAS REPAIRED AND RETURNED TO THE CUSTOMER.

Description of Event or Problem · 1

THE CUSTOMER REPORTED THAT AIR WAS NOT REACHING THE MOTOR. THIS IS REPORT 1 OF 1 FOR COMPLAINT #(B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
662369 LOW PRESS BLACK MAX HANDPIECE MOTOR, DRILL, PNEUMATIC HBB DEPUY SYNTHES POWER TOOLS

Patients

Seq Age Sex Outcome Treatment
1