Catalog Number 4C8723 |
Device Problem
Fitting Problem (2183)
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Patient Problem
No Patient Involvement (2645)
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Event Type
malfunction
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Manufacturer Narrative
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(b)(4).The device was received and is currently awaiting evaluation.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 the connector of a clearlink blood recipient set would not properly connect because the collar would not move into place.There was no patient involvement.No additional information is available.
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Manufacturer Narrative
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(b)(4).The device was received for evaluation.Visual inspection revealed that the collar of the male luer was malformed.The reported condition was verified.The cause of the condition was determined to be due to a manufacturing issue.This issue is being further investigated.Should additional relevant information become available, a supplemental report will be submitted.
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Search Alerts/Recalls
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