FDA Adverse Event Injury Summary report: N

ANESTHESIA MACHINE

MDR report key: 2243988 · Received September 7, 2011

Report

Report Number
MW5022163
Event Type
Injury
Date Received
September 7, 2011
Date of Event
August 30, 2011
Report Date
September 1, 2011
Manufacturer
DATEX-OHMEDA
Product Code
BSZ
Report Source
Voluntary report
Reporter Location
PA, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

DURING PROCEDURE, VENTILATOR FAILURE NOTED. STAFF ABLE TO HAND VENTILATE PATIENT UNTIL EQUIPMENT WAS SWITCHED FOR A DIFFERENT VENTILATOR. PROCEDURE COMPLETED. A REPRESENTATIVE FROM THE COMPANY IS COMING TO SERVICE THE EQUIPMENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ANESTHESIA MACHINE BSZ DATEX-OHMEDA 43902

Patients

Seq Age Sex Outcome Treatment
1 74 YR Required Intervention