The system was used for treatment.This case is reportable as a mdr due to the reportable malfunction tubing leak.Since this reportable malfunction is only associated with the kit, this mdr will only be against the kit.A batch record review for kit lot m123 was conducted.There were no non-conformances associated with this lot.This lot met all release requirements.A review of kit lot m123 shows no trends.Trends were reviewed for complaint category, tubing leak.No trends were detected for this complaint category.At the time of this report, the analysis of the returned kit is still in process.A final report will be filed when the analysis is complete.(b)(4).
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