Patient information was not provided.Livanova (b)(4) manufactures the centrifugal pump system with tubing clamp.The incident occurred in (b)(6).The defective centrifugal pump system with tubing clamp was returned to livanova (b)(4) for investigation.During the investigation the reported failure could not be reproduced.However, during the testing phase the issue that no flow was displayed could be experienced which can be considered as a similar issue.A defective flow board was identified as root cause for this issue.If any additional information pertinent to the reported event is received, it will be provided in a supplemental report.
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