inforMED
InjuryKRR

JOURNEY PFJ IMPLANT X-SM RT

Received Feb 11, 2019 · Event occurred Jan 14, 2019

Report 1020279-2019-00506 · MDR key 8326056

Device

Generic name

Prosthesis, Knee, Patello/femoral, Semi-constrained, Cemented, Metal/polymer

Catalog number

71461011

Product problems

  • Insufficient Device Problem Information
  • Insufficient Device Problem Information

Patient

76 YR

  • Injury
  • Injury

Narrative

Additional Manufacturer Narrative

THE ASSOCIATED COMPLAINT DEVICE WAS NOT RETURNED. THE CLINICAL/MEDICAL TEAM CONCLUDED, NO RELEVANT CLINICAL MEDICAL INFORMATION WAS PROVIDED TO CONDUCT A THOROUGH MEDICAL ASSESSMENT. WITHOUT THE ACTUAL PRODUCT INVOLVED, OUR INVESTIGATION CANNOT PROCEED. IF THE DEVICE OR NEW INFORMATION IS RECEIVED IN THE FUTURE, THIS COMPLAINT CAN BE RE-OPENED. WE CONSIDER THIS INVESTIGATION CLOSED.

Description of Event or Problem

IT WAS REPORTED THAT A REVISION SURGERY WAS PERFORMED TO REMOVE AN IMPLANT.