FDA Adverse Event Summary report: N

BAXTER

MDR report key: 666051 · Received January 11, 2006

Report

Report Number
MW1037740
Date Received
January 11, 2006
Date of Event
December 27, 2005
Report Date
January 11, 2006
Manufacturer
BAXTER HEALTHCARE CORP
Product Code
EYZ
Report Source
Voluntary report
Reporter Location
SC, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

INSERT FOUND IN TUBING. TUBING REMOVED FROM CASE AND ANOTHER SET USED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BAXTER Y TYPE TUR IRRIGATION SET EYZ BAXTER HEALTHCARE CORP 2C4005 *

Patients

Seq Age Sex Outcome Treatment
1 *