Catalog Number 2C6714 |
Device Problems
Crack (1135); Fluid/Blood Leak (1250)
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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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(b)(4).Should additional relevant information become available, a supplemental report will be submitted.
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Event Description
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It was reported that a y-type blood/solution set leaked from a crack at the y-site location.It was not specified when in the process this occurred.There was no report of patient injury or medical intervention associated with this event.No additional information is available.
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Manufacturer Narrative
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(b)(4).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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