FDA Adverse Event Malfunction Summary report: N

AESPIRE VIEW

MDR report key: 8789318 · Received July 15, 2019

Report

Report Number
2112667-2019-00284
Event Type
Malfunction
Date Received
July 15, 2019
Report Date
July 15, 2019
Manufacturer
DATEX-OHMEDA, INC.
Product Code
BSZ
Report Source
Manufacturer report
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

FOR THE REPORTED EVENT, A GE HEALTHCARE SERVICE REPRESENTATIVE PERFORMED A CHECKOUT OF THE SYSTEM AND CONFIRMED THE REPORTED EVENT. THE BYPASS IN THE C02 ABSORBER WAS REPLACED WAS REPLACED TO RESOLVE THE REPORTED ISSUE.

Description of Event or Problem · 1

THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT. A REVIEW OF THE EVENT INDICATED THAT MODEL 1009-9212-000 ANESTHESIA GAS MACHINE EXPERIENCED A DAMAGED CO2 ABSORBER PREVENTING ALL MODES OF VENTILATION. THE REPORT WAS RECEIVED FROM A SINGLE SOURCE. THE REPORTED EVENT DID NOT INVOLVE A PATIENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
584744 AESPIRE VIEW ANESTHESIA GAS MACHINE BSZ DATEX-OHMEDA, INC. 1009-9212-000

Patients

Seq Age Sex Outcome Treatment
1