Device Problems
Device Slipped (1584); Mechanical Jam (2983)
Patient Problem
Insufficient Information (4580)
Event Type
malfunction
Manufacturer Narrative
Identifying information, such as the part number and lot number of the device was not reported to paragon 28.Case information including facility, surgery date(s), or related patient information was not provided by the initial reporter.Devices are not expected to be returned for the manufacturer review/investigation.If any further information is found which would change or alter any conclusions or information, a supplemental report will be filed accordingly.
Event Description
It was reported that during a surgical procedure, a drill guide was stuck to the drill and pulled out of the drill guide.This report is 2 of 2 for this incident.This complaint addresses the drill.