ELEOS¿ LIMB SALVAGE SYSTEM
Received Jul 16, 2026 · Event occurred Jun 15, 2026
Report 3013450937-2026-00258 · MDR key 25838976
Device
Generic name
Eleos¿ Male-female Midsection 50mm
Manufacturer
Onkos Surgical Inc.Catalog number
25001050E
Lot number
1986496
Product problems
- Adverse Event Without Identified Device or Use Problem
Patient
23 YR · Male
- Medical device site infection
Narrative
Additional Manufacturer Narrative
THE ROOT CAUSE OF THIS COMPLAINT WAS NOT DETERMINED. BASED ON THE REVIEW OF KNOWN DEVICE HISTORY RECORDS, THE INVESTIGATION CONCLUDED THAT THE ROOT CAUSE OF THE ALLEGED INFECTION WAS NOT RELATED TO THE DESIGN, MANUFACTURE, AND/OR STERILIZATION OF THE REVISED IMPLANTS.
Description of Event or Problem
IT WAS REPORTED BY AN ONKOS SALES REPRESENTATIVE, THAT A PATIENT WITH ELEOS DISTAL FEMUR REPLACEMENT UNDERWENT REVISION SURGERY ON (B)(6) 2026 DUE TO AN ALLEGED INFECTION. THIS REPORT CAPTURES ELEOS MALE-FEMALE MIDSECTION. THIS EVENT WILL BE REPORTED AS A SERIOUS INJURY DUE TO THE REVISION PROCEDURE.