FDA Adverse Event Injury Summary report: N

VNGD TI FEM CR 60MM LT

MDR report key: 6191319 · Received December 20, 2016

Report

Report Number
0001825034-2016-05328
Event Type
Injury
Date Received
December 20, 2016
Date of Event
November 21, 2016
Report Date
February 14, 2017
Manufacturer
BIOMET ORTHOPEDICS
Product Code
JWH
PMA / PMN Number
PK080204
Removal / Correction Number
N/A
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MS, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

NO DEVICES WERE RECEIVED; THEREFORE THE CONDITION OF THE COMPONENTS IS UNKNOWN. REVIEW OF DEVICE HISTORY RECORDS FOUND NO ANOMALY DURING THE MANUFACTURING PROCESS. THIS DEVICE IS USED FOR TREATMENT. ROOT CAUSE WAS DUE TO PATIENT EXPERIENCING OUTSIDE TRAUMA FROM A CAR ACCIDENT. NO CORRECTIVE ACTIONS, PREVENTIVE ACTIONS, OR FIELD ACTIONS RESULTED AFTER INVESTIGATION OF THIS EVENT.

Additional Manufacturer Narrative · 1

CONCOMITANT PRODUCT(S): - VANGUARD CRUCIATE RETAINING BEARING CATALOG 183546 LOT 722650; BIOMET TIBIAL TRAY CATALOG 141513 LOT 048510. THIS REPORT IS NUMBER 3 OF 4 MDRS FILED FOR THE SAME PATIENT (REFERENCE 1825034-2015-03725 / 1825034-2015-03726 / 1825034-2016-05328 / 1825034-2016-05329).

Description of Event or Problem · 1

PATIENT UNDERWENT A LEFT KNEE REVISION PROCEDURE APPROXIMATELY TWO YEARS POST IMPLANTATION DUE TO LOOSENING CAUSED BY TRAUMA EXPERIENCED BY THE PATIENT. THE BEARING, FEMORAL, AND TIBIAL COMPONENTS WERE REMOVED AND REPLACED; THE FEMORAL COMPONENT WAS REVISED BECAUSE THE SURGEON NOTICED IT WAS 12 DEGREES VALGUS AND HE PREFERRED IT TO BE 5.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
841161 VNGD TI FEM CR 60MM LT CUSTOM TITANIUM VANGUARD CR FEMORAL /ION IMPLANT 60MM LEFT ¿ INTERLOK JWH BIOMET ORTHOPEDICS N/A 701620

Patients

Seq Age Sex Outcome Treatment
1 68 YR Hospitalization| R