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 00,01 report with the FDA on 2013-01-28 for DIGITAL RETINAL CAMERA CX-1 3940B008AA manufactured by Canon Inc..

Event Text Entries

[3132626] The customer reported that there was a shadow on the left side of the image. No information was provided regarding what image types (color, red-free, fluorescein angiography) were affected. The customer did not state that the fluorescein imaging was repeated. However, if the problem occurred during the fluorescein imaging portion of the exam, the technician may have rescheduled the exam. A rescheduled exam would have involved a repeat injection of fluorescein.
Patient Sequence No: 1, Text Type: D, B5


[10509198] 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 dealer service representative replaced the split drive assembly and the main board. The system is working fine now. (b)(4).
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1000181430-2013-00026
MDR Report Key2980370
Report Source00,01
Date Received2013-01-28
Date of Report2011-12-01
Date Mfgr Received2011-12-01
Device Manufacturer Date2007-11-01
Date Added to Maude2013-03-15
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
Manufacturer Street30-2 SHIMOMARUKO, 3-CHOME
Manufacturer CityOHTA-KU, TOKYO 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
Model NumberCX-1
Catalog Number3940B008AA
Lot NumberNA
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerCANON INC.
Manufacturer AddressTOKYO 146-8501 146-8501


Patients

Patient NumberTreatmentOutcomeDate
10 2013-01-28

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