APEX

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2012-11-22 for APEX manufactured by Elekta Ltd..

Event Text Entries

[45582362] From the results of the investigation, apex (collimation head) was incorrectly fitted on to the head of the linac. The rotation of the gantry was prevented by an inhibit, but the user decided to override the inhibit and rotate the linac gantry. The apex detached from the head and hit the floor.
Patient Sequence No: 1, Text Type: N, H10


[45582363] While performing test on apex the system became detached from the linac head during gantry rotation. There has been no injury as a consequence of the incident, but significant damage was sustained to the equipment.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9617016-2012-00007
MDR Report Key5666158
Date Received2012-11-22
Date of Report2012-11-22
Date of Event2012-10-22
Date Added to Maude2016-05-19
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationPHYSICIST
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer StreetFLEMING WAY
Manufacturer CityCRAWLEY
Manufacturer CountryUK
Manufacturer G1ELEKTA LTD.
Manufacturer StreetFLEMING WAY
Manufacturer CityCRAWLEY
Manufacturer CountryUK
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameAPEX
Generic NameBLOCK, BEAM-SHAPING, RADIATION THERAPY
Product CodeIXI
Date Received2012-11-22
Device AvailabilityY
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerELEKTA LTD.
Manufacturer AddressLINAC HOUSE, FLEMING WAY CRAWLE, WEST SUSSEX RH109RR UK RH10 9RR


Patients

Patient NumberTreatmentOutcomeDate
10 2012-11-22

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