FDA Adverse Event
Malfunction
Summary report: N
*
MDR report key: 146256
·
Received October 10, 1996
Report
- Report Number
- 1824226-1996-90002
- Event Type
- Malfunction
- Date Received
- October 10, 1996
- Date of Event
- September 18, 1996
- Manufacturer
- KING SYSTEMS CORP.
- Product Code
- CAI
- Report Source
- Manufacturer report
- Reporter Location
- PA, US
- Reporter Occupation
- INVALID DATA
Narratives
Description of Event or Problem · 1
PT WAS NOT RECEIVING APPROPRIATE VENTILATION WHILE ANESTHESIA CIRCUIT WAS IN USE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | * | * | CAI | KING SYSTEMS CORP. | F345-136 | 1558G6 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * |