FDA Adverse Event Injury Summary report: N

DEVILBLISS SUCTION MACHINE

MDR report key: 2932570 · Received January 25, 2013

Report

Report Number
MW5028746
Event Type
Injury
Date Received
January 25, 2013
Date of Event
December 3, 2013
Report Date
December 17, 2013
Product Code
JCX
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
NJ, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

VENTILATOR DEPENDENT CHILD REQUIRED TRACHEAL SUCTIONING; DEVILBLISS SUCTION UNIT (MODEL #7314P-D) UTILIZED FOR SUCTIONING; DURING TRACHEAL SUCTIONING, MACHINE AUTOMATICALLY SHUT OFF AND LOST SUCTION POWER; HAD TO SWITCH TO ANOTHER DEVILBLISS SUCTION UNIT (MODEL #7305D-D) IN ORDER TO CLEAR THE SECRETIONS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
36083 DEVILBLISS SUCTION MACHINE SUCTION MACHINE JCX 7314P-D
36084 DEVILBLISS SUCITON MACHINE SUCTION MACHINE JCX 7305D-D

Patients

Seq Age Sex Outcome Treatment
1 11 YR Life Threatening| R