FDA Adverse Event
Malfunction
Summary report: N
AESPIRE VIEW
MDR report key: 8515386
·
Received April 15, 2019
Report
- Report Number
- 2112667-2019-00117
- Event Type
- Malfunction
- Date Received
- April 15, 2019
- Report Date
- April 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 EQUIPMENT AND CONFIRMED THE REPORTED EVENT. THE FLOW SENSORS WERE 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 LOSS OF THE ABILITY TO MECHANICALLY VENTILATE IN PRESSURE MODE. THE REPORT WAS RECEIVED FROM A SINGLE SOURCE. THE REPORTED EVENT INVOLVED A PATIENT. THERE WAS NO PATIENT INFORMATION AVAILABLE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 309947 | AESPIRE VIEW | ANESTHESIA GAS MACHINE | BSZ | DATEX-OHMEDA, INC. | 1009-9212-000 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |