FDA Adverse Event
Injury
Summary report: N
DRAEGER
MDR report key: 6793991
·
Received August 11, 2017
Report
- Report Number
- MW5071561
- Event Type
- Injury
- Date Received
- August 11, 2017
- Date of Event
- July 31, 2017
- Report Date
- August 11, 2017
- Manufacturer
- DRAEGER, INC.
- Product Code
- CBK
- Product Problem
- Yes
- Report Source
- Voluntary report
- Reporter Location
- AR, US
- Reporter Occupation
- NURSE
Narratives
Description of Event or Problem · 1
VENTILATOR SHUTDOWN WHILE ATTACHED TO PATIENT. PATIENT WAS DISCONNECTED AND O2 DELIVERED PER AMBU BAG UNTIL ANOTHER VENTILATOR WAS SET UP.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 569837 | DRAEGER | VENTILATOR | CBK | DRAEGER, INC. | 500 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 37 YR | Life Threatening |