FDA Adverse Event Other Summary report: N

4FR V-CATH

MDR report key: 384487 · Received March 21, 2002

Report

Report Number
MW1024465
Event Type
Other
Date Received
March 21, 2002
Manufacturer
HDC CORP
Product Code
DQO
Report Source
Voluntary report
Reporter Occupation
UNKNOWN

Narratives

Description of Event or Problem · 1

AFTER 1 WEEK THE 4FR V-CATH. PICC HAD DEVELOPED HOLE NEAR CATH EXIT SITE AND HAD TO BE PULLED. OTHERWISE CATH INTACT WITHOUT INCIDENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 4FR V-CATH PICC LINE DQO HDC CORP * 1117

Patients

Seq Age Sex Outcome Treatment
1 30 YR Other