The product was not returned for evaluation.Without the return of the device, the root cause of the problem cannot be determined.The manufacturing records for this lot were reviewed and did not reveal any outstanding discrepancies, design, or quality concerns.The hospital disposed of the device.
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During preparation for a coil embolization procedure, the physician noticed that the ruby coil pusher assembly was bent upon removal from its packaging.The bent pusher assembly was found prior to use and therefore, the ruby coil was not used for the procedure.The procedure was completed using a new ruby coil.
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