FDA Adverse Event Injury Summary report: N

CENTERMARK CATHETER

MDR report key: 34826 · Received July 16, 1996

Report

Report Number
34826
Event Type
Injury
Date Received
July 16, 1996
Date of Event
July 5, 1996
Report Date
July 16, 1996
Manufacturer
MENLO CARE, INC.
Product Code
DQO
Adverse Event
Yes
Report Source
User Facility report
Reporter Location
WA, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

PICC LINE PLACED. LINE BEING SLOWLY ADVANCED SUCCESSFULLY. PT C/O BEING "DIZZY" AND FLUSHED, C/O SHORTNESS OF BREATH, BECAME HYPOTENSIVE. PT SENT TO ICU. CATH REMOVED. PT STABILIZED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CENTERMARK CATHETER CATHETER DQO MENLO CARE, INC.

Patients

Seq Age Sex Outcome Treatment
1 62 YR Required Intervention