FDA Adverse Event Summary report: N

OXYGEN SUPPLY TUBING

MDR report key: 32409 · Received April 29, 1996

Report

Report Number
MW4001158
Date Received
April 29, 1996
Date of Event
March 22, 1996
Report Date
March 29, 1996
Manufacturer
HOSPITAK, INC.
Product Code
CAT
Adverse Event
Yes
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
MD, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

NURSING PERSONNEL DISCOVERED EXTENSION TUBE FROM WALL OXYGEN CONNECTED TO IV PORT. RESUSCITATION ATTEMPTED. PT DIED. RPTR SUGGESTS COLOR CODING OF OXYGEN AND IV TUBING AND THAT THEY BE MADE INCOMPATIBLE IN SIZE. (ALSO SEE 4001159).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 OXYGEN SUPPLY TUBING OXYGEN CANNULA CAT HOSPITAK, INC.

Patients

Seq Age Sex Outcome Treatment
1 83 YR Death