FDA Adverse Event Injury Summary report: N

CONNECTOR

MDR report key: 21342 · Received April 14, 1995

Report

Report Number
21342
Event Type
Injury
Date Received
April 14, 1995
Report Date
April 6, 1995
Manufacturer
PHARMASEAL DIV. BAXTER HEALTHCARE CORP.
Product Code
CAI
Product Problem
Yes
Report Source
User Facility report
Reporter Location
CA, US
Reporter Occupation
RESPIRATORY THERAPIST

Narratives

Description of Event or Problem · 1

NURSE STATED VENTILATOR CIRCUIT FELL APART AND SHE WAS ATTEMPTING TO HOLD THE CIRCUIT TOGETHER UNTIL RPTR ARRIVED. RPTR DISCOVERED THAT THE ADAPTER HAD SEPARATED INTO TWO PIECES AND IT WAS AT THE SEPARATION POINT THAT THERE WAS A BREAK IN THE VENTILATOR CIRCUIT. PROBLEM WAS QUICKLY CORRECTED AND PT SUFFERED NO ILL EFFECTS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CONNECTOR VENT/TRACK CONNECTOR CAI PHARMASEAL DIV. BAXTER HEALTHCARE CORP. 3222 F5C61161, F5B46821

Patients

Seq Age Sex Outcome Treatment
1 68 YR Life Threatening| R