FDA Adverse Event
Summary report: N
PHILIPS HEALTHCARE V-60 NON-INVASIVE VENTILATOR
MDR report key: 7147609
·
Received December 26, 2017
Report
- Report Number
- MW5074240
- Date Received
- December 26, 2017
- Date of Event
- December 18, 2017
- Report Date
- December 21, 2017
- Manufacturer
- PHILIPS HEALTHCARE NORTH AMERICA
- Product Code
- CBK
- UDI-DI
- 0108924496
- Report Source
- Voluntary report
- Reporter Location
- OH, US
- Reporter Occupation
- UNKNOWN
Narratives
Description of Event or Problem · 1
WHILE TRANSFERRING THE PATIENT PROCEDURE, THE VENTILATOR SHUT DOWN AND WENT INOPERATIVE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 925032 | PHILIPS HEALTHCARE V-60 NON-INVASIVE VENTILATOR | VENTILATOR | CBK | PHILIPS HEALTHCARE NORTH AMERICA | V60 | 0108924496 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 41 YR |