InjuryKRR
UNKNOWN_TRIATHLON TIBIAL INSERT
Received Oct 19, 2016 · Event occurred Sep 22, 2016
Report 0002249697-2016-03289 · MDR key 6042071
Device
Generic name
Knee Implant
Manufacturer
Stryker Orthopaedics-mahwahCatalog number
UNK_REC
Lot number
UNKNOWN
Product problems
- Insufficient Device Problem Information
- Insufficient Device Problem Information
Patient
56 YR
- Injury
- Injury
Narrative
Additional Manufacturer Narrative
AN EVALUATION OF THE DEVICE CANNOT BE PERFORMED AS THE DEVICE WAS NOT RETURNED TO THE MANUFACTURER DUE TO HOSPITAL POLICY. ADDITIONAL INFORMATION HAS BEEN REQUESTED. SHOULD ADDITIONAL INFORMATION BECOME AVAILABLE IT WILL BE REPORTED IN A SUPPLEMENTAL REPORT UPON COMPLETION OF THE INVESTIGATION. NOT RETURNED TO THE MANUFACTURER.
Description of Event or Problem
PATIENT HAD LEFT KNEE REVISION.