FDA Adverse Event Injury Summary report: N

AVANTAGE CUP

MDR report key: 8266292 · Received January 22, 2019

Report

Report Number
3006946279-2019-00063
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 HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

(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, IT CANNOT BE DETERMINED IF A ZIMMER BIOMET PRODUCT WAS INVOLVED IN THIS EVENT AND 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.

Description of Event or Problem · 1

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
58990 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