UNKNOWN OXFORD KNEE BEARING
Report
- Report Number
- 3002806535-2017-00654
- Event Type
- Injury
- Date Received
- August 10, 2017
- Date of Event
- May 10, 2017
- Report Date
- August 9, 2017
- Manufacturer
- BIOMET UK LTD.
- Product Code
- NRA
- PMA / PMN Number
- PP010014
- Removal / Correction Number
- N/A
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CH
- Reporter Occupation
- PHYSICIAN
Narratives
(B)(4). REPORT SOURCE, FOREIGN ¿ EVENTS OCCURRED IN (B)(6). REPORT SOURCE, LITERATURE - XUE, H. ET AL (2017). UP TO TWELVE YEAR FOLLOW-UP OF THE OXFORD PHASE THREE UNICOMPARTMENTAL KNEE REPLACEMENT IN CHINA: SEVEN HUNDRED AND EIGHT KNEES FROM AN INDEPENDENT CENTRE. INTERNATIONAL ORTHOPAEDICS, 41(8),1571¿1577. DOI 10.1007/S00264-017-3492-4. REPORTED EVENT WAS UNABLE TO BE CONFIRMED DUE TO LIMITED INFORMATION RECEIVED FROM THE CUSTOMER. DEVICE HISTORY RECORD (DHR) REVIEW WAS UNABLE TO BE PERFORMED AS THE LOT NUMBER OF THE DEVICE INVOLVED IN THE EVENT IS UNKNOWN. ROOT CAUSE WAS UNABLE TO BE DETERMINED. IF ANY FURTHER INFORMATION IS FOUND WHICH WOULD CHANGE OR ALTER ANY CONCLUSIONS OR INFORMATION, A SUPPLEMENTAL WILL BE FILED ACCORDINGLY. ZIMMER BIOMET WILL CONTINUE TO MONITOR FOR TRENDS. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 3002806535-2017-00655, 3002806535-2017-00656.
IT HAS BEEN REPORTED IN A JOURNAL ARTICLE THAT A PATIENT UNDERWENT A REVISION DUE TO PERSISTENT PAIN 4.1 YEARS AFTER THE INITIAL PROCEDURE. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 566957 | UNKNOWN OXFORD KNEE BEARING | PROSTHESIS, KNEE | NRA | BIOMET UK LTD. | N/A | NI |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Hospitalization| R | UNKNOWN OXFORD FEMORAL COMPONENT| UNKNOWN OXFORD TIBIAL COMPONENT |