Patient demographics (date of birth, weight) were requested but not provided.No further patient information was provided at the time of this report or made available in response to follow-up communication.No additional adverse consequences have been reported from this event.This device is used for treatment.The partial device was received and an evaluation was conducted.The complaint was not confirmed.Device history record review revealed nothing relevant to this event.The returned device consisted of the driver and sutures only.Pieces of the implant were not returned for evaluation.A definitive cause of the event could not be determined without device evaluation.However, based on the event description the complainant's event was most likely caused by not inserting the implant co-axial to the bone tunnel or prying/leveraging the driver while the implant is still loaded, over-insertion, improper bone preparation or insertion into hard bone.This is the first complaint of this type for this part/lot combination.The potential cause(s) of this event will be communicated to the event reporter.If additional relevant information is received, a follow-up report will be submitted.
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