FDA Adverse Event Injury Summary report: N

UNKNOWN KNEE

MDR report key: 4943611 · Received July 27, 2015

Report

Report Number
0001825034-2015-03290
Event Type
Injury
Date Received
July 27, 2015
Report Date
July 10, 2015
Manufacturer
BIOMET ORTHOPEDICS
Product Code
NRA
PMA / PMN Number
PUNKNOWN
Removal / Correction Number
N/A
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
BE
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

CURRENT INFORMATION IS INSUFFICIENT TO PERMIT CONCLUSIONS AS TO THE CAUSE OF THE EVENTS. EVENT DETAILS AND PRODUCT IDENTIFICATION WAS NOT PROVIDED FOR THE PATIENTS MENTIONED IN THE JOURNAL ARTICLE. THE ARTICLE WAS WRITTEN BY VORLAT P, ET AL IN KNEE SURG SPORTS TRAUMATOL ARTHROSC. 2006 JAN;14(1):40-5. IT IS LIKELY THAT THESE COMPLICATIONS AND REVISIONS HAVE ALREADY BEEN REPORTED; HOWEVER, IT CANNOT BE DETERMINED BASED ON THE LIMITED INFORMATION MADE AVAILABLE IN THE ARTICLE. SHOULD ADDITIONAL INFORMATION RELATING TO THE EVENTS BE RECEIVED, THE UPDATED INFORMATION WILL BE FORWARDED TO THE FDA. THIS INFORMATION WAS ORIGINALLY REPORTED ON 1825034-2015-03285 WHICH REFERENCED A JOURNAL ARTICLE WRITTEN ON A STUDY THAT THIS PATIENT TOOK PART IN.

Description of Event or Problem · 1

INFORMATION WAS RECEIVED BASED ON REVIEW OF A JOURNAL ARTICLE TITLED, "THE OXFORD UNICOMPARTMENTAL KNEE PROSTHESIS: AN INDEPENDENT 10-YEAR SURVIVAL ANALYSIS" VORLAT, P. ET AL. KNEE SURG SPORTS TRAUMATOL ARTHROSC (2006) 14: 40-45 DOI: 10.1007/S00167-005-0621-1. IT WAS REPORTED THAT PATIENT UNDERWENT A PARTIAL KNEE ARTHROPLASTY ON AN UNKNOWN SIDE ON AN UNKNOWN DATE. SUBSEQUENTLY, PATIENT WAS REVISED DUE TO MENISCUS FRACTURE 119 MONTHS FOLLOWING THE INITIAL PROCEDURE. THE TIBIAL BEARING WAS REMOVED AND REPLACED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
485919 UNKNOWN KNEE PROSTHESIS, KNEE NRA BIOMET ORTHOPEDICS N/A UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization| R