Correction: section initial reporter health professional.The reported incident could not be confirmed, since the inspection of the device showed that the length of the device is indeed a 19mm and that the part is conform to the manufacturing specifications.Therefore, based on the inspection of the device, we can confirm that there is no mix up, and that the implant is indeed the reference mentioned in the packaging.A review of the device history for the reported lot did not indicate any abnormalities.No corrective actions are required at this time.A review of the labeling did not indicate any abnormalities.No indications of material, manufacturing or design related problems were found during the investigation.
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