VNGD TI FEM CR 60MM LT
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
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.
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).
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 |