A pair of expired anchors was reported to abbott.Although the anchors were present during the operation, abbott advised against the implantation of the anchors, but the effort was unsuccessful.Based on the information received, the event is consistent with the unintentional use of expired product.Additionally, the device history record of the device was reviewed to confirm that all manufacturing steps were completed and there were no non-conformances noted that could have contributed to this issue.Actions have been taken to prevent reoccurrence via capa 132510.The anchors were ultimately removed and replaced with new anchors to resolve the issue.
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