FDA Adverse Event Malfunction Summary report: N

DIALYSIS ADMINISTRATION SET

MDR report key: 39627 · Received September 24, 1996

Report

Report Number
MW1009979
Event Type
Malfunction
Date Received
September 24, 1996
Date of Event
August 22, 1996
Report Date
September 12, 1996
Manufacturer
BAXTER HEALTHCARE CORP.
Product Code
FJX
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
MI, US
Reporter Occupation
OTHER CAREGIVERS

Narratives

Description of Event or Problem · 1

NO CLAMP ON VENOUS TUBE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 DIALYSIS ADMINISTRATION SET DIALYSIS ADMINISTRATION SET FJX BAXTER HEALTHCARE CORP. 5M4484M YGE099

Patients

Seq Age Sex Outcome Treatment
1 *