FDA Adverse Event Injury Summary report: N

UNKNOWN OXFORD KNEE BEARING

MDR report key: 6784139 · Received August 10, 2017

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

Additional Manufacturer Narrative · 1

(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.

Description of Event or Problem · 1

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