The system was used for treatment.This case is reportable as a mdr due to the reportable malfunction alarm #7: blood leak? (centrifuge chamber).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 k167 was conducted.There were no non-conformances associated with this lot.This lot met all release requirements.A review of kit lot k167 shows no trends.Trends were reviewed for complaint category, alarm #7: blood leak? (centrifuge chamber).No trends were detected for this complaint category.The assessment is based on the information available at the time of investigation.No product was returned for investigation; therefore, it could not be determined if the product met specification based solely on the information provided by the customer.Complaints are monitored through tracking and trending.If a trend is detected, further investigation will be conducted.No further action is required at this time.This investigation is now complete.(b)(4).
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