FDA Adverse Event
Injury
Summary report: N
HIGH FREQUENCY JET VENT
MDR report key: 18046
·
Received November 30, 1994
Report
- Report Number
- MW1004201
- Event Type
- Injury
- Date Received
- November 30, 1994
- Date of Event
- January 12, 1994
- Manufacturer
- BUNNELL, INC.
- Product Code
- CBK
- Report Source
- Voluntary report
- Reporter Location
- PA, US
- Reporter Occupation
- RISK MANAGER
Narratives
Description of Event or Problem · 1
HIGH FREQUENCY JET VENTILATOR ALARMED FOR LOW PIP. ADJUSTMENTS WERE MADE BUT PIP WAS UNABLE TO BE MET. IT WAS DETERMINED THE PT BOX WAS FAULTY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | HIGH FREQUENCY JET VENT | HIGH FREQUENCY JET VENT | CBK | BUNNELL, INC. |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 4 DAY | Required Intervention |