This report has been identified as event 2 of b.Braun medical internal report number (b)(4).Two (2) unused spinocan needles with packaging were returned for evaluation.The samples were visually inspected and foreign material was identified in the packaging of both samples.Retained units for batch number 0061681018 were inspected, and no defects were noted.Although the reported defect was confirmed, the exact root cause was unable to be determined.Review of the discrepancy management system (dsms) database performed for the reported lot number revealed no abnormalities or non conformances noted during in process or final product inspection.If any additional pertinent information becomes available, a follow-up will be submitted.
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