Catalog Number 1C8740 |
Device Problem
Defective Device (2588)
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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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Should additional relevant information become available, a supplemental report will be submitted.
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Event Description
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This report summarizes 1 malfunction events.It was reported that one interlink minivolume extension set was ¿defective¿.This occurred during an unspecified process step.It is unknown if a patient was involved in the event.No additional information is available.
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Manufacturer Narrative
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Additional information: the device was not returned and the lot number is unknown; therefore, a device analysis could not be completed.Should additional relevant information become available, a supplemental report will be submitted.
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Search Alerts/Recalls
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