Model Number CLV-S40PRO |
Device Problem
Electrical /Electronic Property Problem (1198)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Type
malfunction
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Manufacturer Narrative
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The subject device was not returned to omsc for evaluation.The exact cause of the reported event could not be conclusively determined at this time.If additional information becomes available, this report will be supplemented.
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Event Description
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Olympus medical systems corp.(omsc) was informed from the user facility that in unspecified timing, the front panel display of the subject device blinked.There was no report of patient injury associated with this event.The user facility did not provide other detailed information.Olympus service operation repair center (sorc) checked the subject device and found that the front panel display blinked due to the malfunction of the filter turret.
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Manufacturer Narrative
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This supplemental report is being submitted to provide additional information.The subject device was not returned to olympus medical systems corp.(omsc) for evaluation.Omsc reviewed the manufacturing history (dhr) of the subject device and confirmed no irregularity.The exact cause of the reported phenomenon could not be conclusively determined.However, based upon the information from olympus service operation repair center (sorc), there was the possibility that the reported phenomenon was attributed to the aging deterioration of the mesh turret or the filter turret motors due to repeatedly use for a long-term use because more than 13 years had passed from the subject device had been manufactured.
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Search Alerts/Recalls
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