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 |