FDA Adverse Event Injury Summary report: N

PURITAN BENNETT

MDR report key: 1011354 · Received March 10, 2008

Report

Report Number
MW5005849
Event Type
Injury
Date Received
March 10, 2008
Date of Event
March 6, 2008
Report Date
March 10, 2008
Manufacturer
PURITAN BENNETT
Product Code
CBK
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
NM, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

PT VISIBLY TRYING TO TAKE SPONTANEOUS BREATHS, BUT COULD NOT TRIGGER VENT ABOVE SET RESPIRATION RATE. GRAPHICS DISPLAY SHOWED EFFORTS ADEQUATE TO TRIGGER BREATHS, BUT VENT DID NOT DELIVER. SWITCHED TO ANOTHER VENT & PT WAS ABLE TO TRIGGER BREATHS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PURITAN BENNETT 7200 VENTILATOR CBK PURITAN BENNETT 7200

Patients

Seq Age Sex Outcome Treatment
1 Disability