FDA Adverse Event Injury Summary report: N

BCS TIBIA BASE PLATE

MDR report key: 3092638 · Received May 3, 2013

Report

Report Number
1020279-2013-00247
Event Type
Injury
Date Received
May 3, 2013
Date of Event
December 23, 2012
Report Date
April 23, 2013
Manufacturer
SMITH & NEPHEW, INC.
Product Code
JWH
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

.

Description of Event or Problem · 1

PATIENT WAS ADMITTED INTO THE HOSPITAL FOR BLEEDING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
193951 BCS TIBIA BASE PLATE JOURNEY TIBIA BASE NP LT SZ 5 JWH SMITH & NEPHEW, INC. 12EM04573

Patients

Seq Age Sex Outcome Treatment
1 63 YR Hospitalization 71332535/12GM01806| 74027262/12AM10967| 74024838/12FM00231| 74022125/12EM00472| 71332535/12HM12059