AVANTAGE CUP
Report
- Report Number
- 3006946279-2019-00061
- Event Type
- Injury
- Date Received
- January 22, 2019
- Date of Event
- December 2, 2017
- Report Date
- January 22, 2019
- Manufacturer
- BIOMET FRANCE S.A.R.L.
- Product Code
- JDL
- PMA / PMN Number
- N/A
- Removal / Correction Number
- N/A
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- LH
- Reporter Occupation
- OTHER
Narratives
(B)(4). REPORT SOURCE : JOURNAL ARTICLE, FOREIGN - EVENT OCCURRED IN (B)(6). REFERENCE: STUCINSKAS, JUSTINAS, KALVAITIS, TOMAS, SMAILYS, ALFREDAS, ROBERTSSON, OTTO & TARASEVICIUSV SARUNAS (2017) COMPARISON OF DUAL MOBILITY CUP AND OTHER SURGICAL CONSTRUTS USED FOR THREE HUNDRED AND SIXTY TWO FIRST TIME HIP REVISIONS DUE TO RECURRENT DISLOCATIONS: FIVE YEAR RESULTS FROM LITHUANIAN ARTHROPLASTY REGISTER. INTERNATIONAL ORTHOPAEDICS 42:1015¿1020.HTTPS://DOI.ORG/10.1007/S00264-017-3702-0. THE DEVICE WAS NOT RETURNED TO THE MANUFACTURER. THEREFORE IT COULD NOT BE ANALYZED THE DEVICE MANUFACTURING QUALITY RECORD COULD NOT BEEN REVIEWED AS THE LOT NUMBER WAS NOT COMMUNICATED. ACCORDING TO THE AVAILABLE DATA, THE EXACT ROOT CAUSE COULD NOT 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. DEVICE NOT RETURNED.
JOURNAL ARTICLE REPORTED THAT PATIENT UNDERWENT REVISION SURGERY DUE TO DISLOCATION ON AVANTAGE CUP.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 59187 | AVANTAGE CUP | PROSTHESIS, HIP, SEMI-CONSTRAINED (METAL CEMENTED ACETABULAR COMPONENT) | JDL | BIOMET FRANCE S.A.R.L. | N/A | NOT COMMUNICATED |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Hospitalization| R |