InjuryJEY
LEVEL ONE CMF
Received Apr 23, 2026
Report 1000525271-2026-00011 · MDR key 24972133
Device
Product problems
- Adverse Event Without Identified Device or Use Problem
Patient
51 YR · Male
- Insufficient Information
Narrative
Additional Manufacturer Narrative
POSSIBLE PRODUCTS IDENTIFIED: 25-860-07-91 LOT 33704706 25-861-05-91 LOT 33573794.
Description of Event or Problem
IT WAS REPORTED THAT A SCREW FIXATING A BSSO PLATE WAS REMOVED SEVEN WEEKS AFTER IMPLANT FOR UNKNOWN REASONS AFTER PATIENT HAD ACHIEVED GOOD BONE CONSOLIDATION. IT WAS NOT REPLACED.