Model Number CYF-5 |
Device Problem
Microbial Contamination of Device (2303)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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Event Type
malfunction
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Manufacturer Narrative
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The subject device in this report has not been returned to omsc for evaluation.Omsc reviewed the manufacturing history of the subject device and confirmed no irregularity.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 that as a result of microbiological testing by the user facility, the sample collected from the subject device tested positive.The device had been manually reprocessed using peracetic acid (perasafe).There was no report of infection associated with this report.
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Manufacturer Narrative
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This supplemental report is being submitted to provide additional information.The subject device has not been returned to olympus medical systems corp.(omsc) but was returned to olympus (b)(4).(b)(4) sent the device to a third party laboratory for microbiological testing.The additional microbiological testing indicated no microbial growth for the all channels of the device.Therefore, the testing result cleared the (b)(4) guideline.The exact cause of the reported event could not be conclusively determined at this time.If additional information is received, this report will be supplemented.
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Search Alerts/Recalls
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