Product complaint # (b)(4).If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.Evaluation statement: the complaint device was received at service center for service and repair.The reported failure could not be duplicated and the complaint cannot be confirmed.Regular maintenance was performed and the worn tips & rubber feet were replaced.The testing of the unit was completed per the service manual.The unit passed all functional tests and is fully operational.A review of batch history for each legacy fms product complaint is not possible since legacy manufacturing no longer exists.At this point in time, no corrective action is required, and no further action is warranted.Depuy 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).Associated medwatch report number: 1221934-2018-54503.
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