DIGITAL RETINAL CAMERA CX-1 3940B008AA

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2013-01-28 for DIGITAL RETINAL CAMERA CX-1 3940B008AA manufactured by Canon, Inc..

Event Text Entries

[3157292] The customer reported that the barrier filter hung between positions, due to the yellow appearance on one arc, and the clear appearance on the other. The info on the barrier filter indicates that they were performing fluorescein angiography at the time of the event. The customer did not mention that they had to re-inject the pt with fluorescein or reschedule the pt exam. However, the info suggests that a repeat injection may have been necessary during the exam, or a reschedule exam, due to barrier filter problem.
Patient Sequence No: 1, Text Type: D, B5


[10440630] This mdr is being submitted retroactively as a result of an internal audit of complaint files conducted by canon healthcare solutions usa. (b)(4). The svc rep repaired the exciter filter turret spring. It had fallen off and left the filter hanging in the optical path. (b)(4).
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1000181430-2013-00024
MDR Report Key2945812
Report Source06
Date Received2013-01-28
Date of Report2010-09-29
Date Mfgr Received2010-09-29
Device Manufacturer Date2008-01-01
Date Added to Maude2013-02-07
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactMR. NAOYASU ASAKA, MGR.
Manufacturer Street30-2 SHIMOMARUKO, 3-CHOME OHTA-KU
Manufacturer CityTOKYO 146-8501
Manufacturer CountryJA
Manufacturer Postal146-8501
Manufacturer Phone37582111
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameDIGITAL RETINAL CAMERA CX-1
Product CodeNFJ
Date Received2013-01-28
Returned To Mfg2010-09-30
Model NumberCX-1
Catalog Number3940B008AA
Lot NumberNA
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerCANON, INC.
Manufacturer AddressTOKYO 146-8501 146-8501


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2013-01-28

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.