FDA Adverse Event
Malfunction
Summary report: N
AS3000 ANESTHESIA SYSTEM
MDR report key: 3091325
·
Received April 30, 2013
Report
- Report Number
- 2221819-2013-00188
- Event Type
- Malfunction
- Date Received
- April 30, 2013
- Date of Event
- September 18, 2012
- Report Date
- April 30, 2013
- Manufacturer
- MINDRAY DS USA, INC.
- Product Code
- BSZ
- PMA / PMN Number
- 080175
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- WV, US
- Reporter Occupation
- UNKNOWN
Narratives
Description of Event or Problem · 1
CUSTOMER REPORTED A SYSTEM LEAK ON THE AS3000 ANESTHESIA SYSTEM. NO PATIENT INJURY WAS REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 187302 | AS3000 ANESTHESIA SYSTEM | ANESTHESIA DELIVERY SYSTEM | BSZ | MINDRAY DS USA, INC. |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |