The system was used for treatment.This case is reportable as a mdr due to the reportable malfunction pump tubing organizer (pto) 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 h267 was conducted.There were no non-conformance's associated with this lot.This lot met all release requirements.A review of kit lot h267 shows no trends.Trends were reviewed for complaint category, pto leak.No trends were detected for this complaint category.Photographs were provided by the customer for evaluation.The complaint kit with smart card was not returned.A review of the photographs verify a blood leak on the cellex instrument pump deck.The leak appears to be coming from the location of the pump tubing organizer (pto); however, the exact location of the leak could not be determined based on the photographs.A material trace of components used to build lot h267 did not find any non-conformance's.A device history record (dhr) review did not result in any related non-conformance's and this kit lot passed all lot release testing.The root cause for the pto leak could not be determined based on the available information.No further action is required at this time.This investigation is now complete.(b)(4).
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