FDA Adverse Event Injury Summary report: N

SAF SITE

MDR report key: 13733 · Received June 2, 1994

Report

Report Number
MW1002328
Event Type
Injury
Date Received
June 2, 1994
Date of Event
April 30, 1994
Report Date
May 17, 1994
Manufacturer
B. BRAUN MEDICAL, INC.
Product Code
FPA
Report Source
Voluntary report
Reporter Location
TX, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

PT HEMORRHAGED FROM PERIPHERAL IV SITE AT THE CONNECTION OF IV HUB AND HUB OF Y-CONNECTOR.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SAF SITE SMALL BORE Y EXTENSION SET FPA B. BRAUN MEDICAL, INC.

Patients

Seq Age Sex Outcome Treatment
1 8 DAY Life Threatening