InjuryKWH
IMPLANT, 10MM CLEAR STERILE INTERPHLEX
Received Apr 27, 2026 · Event occurred Apr 14, 2026
Report 2027754-2026-00014 · MDR key 25009561
Device
Generic name
Prosthesis, Toe, Constrained, Polymer
Manufacturer
Osteomed LlcModel number
360-2810Lot number
1168523
Product problems
- Adverse Event Without Identified Device or Use Problem
Patient
NA · Unknown
- No Clinical Signs, Symptoms or Conditions
Narrative
Additional Manufacturer Narrative
IT IS UNCLEAR WHY THE DEVICE WAS USED AFTER IT HAD PASSED ITS EXPIRATION DATE. NO FURTHER ACTION WAS REPORTED AFTER THIS INITIAL INCIDENT. IF ANY ADDITIONAL INFORMATION BECOMES AVAIABLE, IT WILL BE SUBMITTED AS A FOLLOW UP.
Description of Event or Problem
IT WAS REPORTED: A FACILITY HAS INFORMED US THAT AN EXPIRED INTERPHLEX IMPLANT WAS INADVERTENTLY INSERTED INTO A PATIENT. THE INTERPHLEX IMPLANT EXPIRED ON (B)(6) 2026, AND WAS INSERTED ON (B)(6) 2026. ITS BATCH NUMBER IS 1168523.