If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.The defect reported has been verified and repaired.The following repair activities were performed: performed service and repair functions.Reviewed service history.Attach box label, software upgrade form, and fms vue final testing.Reseated loose on door sensor magnet to correct issue.Also replaced broken fill chamber holder.Per service bulletin, performed software upgrade to the latest versions.Per service bulletin, replaced springs on pressure arm housing (preventive maintenance) with tip replacement kit.The unit passed all diagnostic tests, functional tests, and is fully operational.Details can be found in the attached reports.Further, a review into the depuy synthes mitek complaints system revealed no other complaints for this device's serial number.At this point in time, no corrective action is required and no further action is warranted.However, depuy synthes mitek will continue to track any related complaints within this device family as a means of monitoring the extent with which this complaint is observed in the field.Udi: (b)(4).This report is being filed from the etq complaint management system as required under mitek's corrective and preventative actions (capa) to file usa fda mdr missed malfunctions.
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