FDA Adverse Event Malfunction Summary report: N

HEMAQUET EXCEL

MDR report key: 11620 · Received February 18, 1994

Report

Report Number
MW1000832
Event Type
Malfunction
Date Received
February 18, 1994
Date of Event
February 9, 1994
Report Date
February 10, 1994
Manufacturer
USCI DIV. C.R. BARD, INC.
Product Code
DYB
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
FL, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

SHEATH VALVE LEAKED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HEMAQUET EXCEL DYB USCI DIV. C.R. BARD, INC. 09LD0195

Patients

Seq Age Sex Outcome Treatment
1 68 YR Other