FDA Adverse Event Malfunction Summary report: N

ONCENTRA MASTERPLAN

MDR report key: 1076852 · Received July 14, 2008

Report

Report Number
9611894-2008-00011
Event Type
Malfunction
Date Received
July 14, 2008
Date of Event
June 23, 2008
Report Date
July 10, 2008
Manufacturer
NUCLETRON B.V.
Product Code
MUJ
PMA / PMN Number
K081281
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GM
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THIS PROBLEM IS THE SAME AS THE PROBLEMS REPORTED UNDER 9611894-2008-00007 THROUGH 961184-2008-00010. CUSTOMER BULLETIN 555. 00072-01 REVISED INFO: INCONSISTENT DOSE AFTER BEAM WEIGHTING OR AUTO RECOVERY WAS RE-ISSUED TO FACILITIES ON JUNE 24, 2008. IN ADDITION, SERVICE BULLETIN 666.00020-00, STOP ROLL-OUT OF OCENTRA MASTERPLAN FOR ALL EXTERNAL BEAM CUSTOMERS WAS ISSUED ON JUNE 24, 2008.

Description of Event or Problem · 1

THE MU'S ENTERED IN THE WEIGHTING DIALOG DO NOT MATCH THE DOSE DISTRIBUTION. DOSE DISTRIBUTION DOESN'T MATCH SETTINGS IN THE WEIGHTING DIALOG.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ONCENTRA MASTERPLAN MEDICAL CHARGED PARTICLE RADIATION THER MUJ NUCLETRON B.V. 170.700

Patients

Seq Age Sex Outcome Treatment
1