FDA Adverse Event Malfunction Summary report: N

BLACKMAX-NEURO LOW PRESSURE

MDR report key: 4183302 · Received October 17, 2014

Report

Report Number
1045834-2014-14545
Event Type
Malfunction
Date Received
October 17, 2014
Report Date
November 28, 2012
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 OUS 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, RPM BELOW SPECIFICATION WAS FOUND. FUNCTIONAL TESTING WAS PERFORMED AND IMPROPER FUNCTION WAS FOUND; THE CAUSE IS NORMAL WEAR. DEVICE WAS REPAIRED AND RETURNED TO THE CUSTOMER. MANUFACTURING DATE FOR THIS DEVICE IS UNAVAILABLE.

Description of Event or Problem · 1

THE DEVICE WAS RETURNED FOR AN UNSPECIFIED REASON. THIS IS REPORT 1 OF 1 FOR (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
660147 BLACKMAX-NEURO LOW PRESSURE MOTOR, DRILL, PNEUMATIC - HANDPIECE HBB DEPUY SYNTHES POWER TOOLS

Patients

Seq Age Sex Outcome Treatment
1