FDA Adverse Event
Injury
Summary report: N
SERVO
MDR report key: 3830021
·
Received May 19, 2014
Report
- Report Number
- MW5036206
- Event Type
- Injury
- Date Received
- May 19, 2014
- Date of Event
- May 8, 2014
- Report Date
- May 16, 2014
- Manufacturer
- SIEMENS
- Product Code
- CBK
- Product Problem
- Yes
- Report Source
- Voluntary report
- Reporter Location
- CA, US
- Reporter Occupation
- NURSE
Narratives
Description of Event or Problem · 1
PATIENT WAS ON A VENTILATOR. THE VENTILATOR WAS MALFUNCTIONING READING HIGH RESPIRATORY RATE ALARMING. ALARM SHOWING RR IN 60'S. ASSESSMENT SHOWED RR IN 20'S.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 295675 | SERVO | VENTILATOR | CBK | SIEMENS | 6487800 | ||
| 295676 | DISPLAY SCREEN FOR SERVO VENTILATOR | DISPLAY SCREEN FOR SERVO VENTILATOR | CBK | SIEMENS | 6567288 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 68 YR | Hospitalization |