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Catalog Number ASKU |
Device Problems
Fluid/Blood Leak (1250); Material Integrity Problem (2978)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Type
malfunction
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Event Description
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It was reported that two (2) unspecified access sets leaked at the spike site when connected to non-baxter bags.It was not specified when in the process step this occurred.The customer indicated the spike was too short in the tubing.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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Should additional relevant information become available, a supplemental report will be submitted.
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Manufacturer Narrative
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H10: 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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