Initial reporter facility name: (b)(6) hospital.The actual device was not available; however, a video of the sample was provided for evaluation.The returned video was reviewed, and it was confirmed that there was a leak from the stopcock.The reported condition was verified.The cause of the reported condition could not be determined.A batch review was conducted and there were no deviations found related to this reported condition during the manufacture of this lot.Should additional relevant information become available, a supplemental report will be submitted.
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