FDA Adverse Event Injury Summary report: N

BIOMET ARCOM ALL POLY PAT BUTTON

MDR report key: 6357304 · Received February 24, 2017

Report

Report Number
0001825034-2017-00897
Event Type
Injury
Date Received
February 24, 2017
Date of Event
January 24, 2017
Report Date
September 23, 2017
Manufacturer
BIOMET ORTHOPEDICS
Product Code
JWH
PMA / PMN Number
PK921182
Removal / Correction Number
N/A
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MS, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

THIS REPORT IS NUMBER 1 OF 2 MDRS FILED FOR THE SAME PATIENT (REFERENCE 0001825034-2017-00898).

Additional Manufacturer Narrative · 1

THIS FOLLOW-UP REPORT IS BEING SUBMITTED TO RELAY ADDITIONAL INFORMATION. CONCOMITANT MEDICAL PRODUCTS: VANGUARD CR ILOK FEM-LT 75 P/N 183034 L/N 834540, BIOMET CC CRUCIATE TRAY 79 MM P/N 141235 L/N 778010. REPORTED EVENT WAS UNABLE TO BE CONFIRMED. DEVICE HISTORY RECORD WAS REVIEWED AND NO DISCREPANCIES RELEVANT TO THE REPORTED EVENT WERE FOUND. REVIEW OF COMPLAINT HISTORY DETERMINED THAT NO FURTHER ACTION IS REQUIRED AS NO TRENDS WERE IDENTIFIED. ROOT CAUSE WAS UNABLE TO BE DETERMINED. THERE ARE WARNINGS IN THE PACKAGE INSERT THAT THIS TYPE OF EVENT CAN OCCUR AND ASSOCIATED RISKS ARE ADDRESSED IN RISK DOCUMENTATION. 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

IT IS REPORTED THAT THE PATIENT WAS REVISED TO DUE TO A FRACTURED PATELLA COMPONENT AND INSTABILITY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
139471 BIOMET ARCOM ALL POLY PAT BUTTON PROSTHESIS, KNEE JWH BIOMET ORTHOPEDICS N/A 779780

Patients

Seq Age Sex Outcome Treatment
1 54 YR Hospitalization| R 183560 VNGD CR LIP TIB BRG, LOT 547300