FDA Adverse Event
Malfunction
Summary report: N
LP10 VOLUME VENTILATOR
MDR report key: 40180
·
Received September 11, 1996
Report
- Report Number
- 2183157-1996-00021
- Event Type
- Malfunction
- Date Received
- September 11, 1996
- Report Date
- August 12, 1996
- Manufacturer
- AEQUITRON MEDICAL, INC.
- Product Code
- CBK
- Removal / Correction Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IL, US
- Reporter Occupation
- RESPIRATORY THERAPIST
Narratives
Description of Event or Problem · 1
REPORT OF ALLEGED "PRESSURE LIMIT CONTROL VALVE STUCK AND ALARMED. NO PT HARM."
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | LP10 VOLUME VENTILATOR | VOLUME VENTILATOR | CBK | AEQUITRON MEDICAL, INC. | LP10 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * | Other |