FDA Adverse Event
Malfunction
Summary report: N
GAS MODULE III RESPIRATION GAS MONITOR
MDR report key: 3091741
·
Received April 30, 2013
Report
- Report Number
- 2221819-2013-00725
- Event Type
- Malfunction
- Date Received
- April 30, 2013
- Date of Event
- January 15, 2013
- Report Date
- April 30, 2013
- Manufacturer
- MINDRAY DS USA, INC.
- Product Code
- BZK
- PMA / PMN Number
- 062754
- Report Source
- Manufacturer report
- Reporter Location
- DE, US
- Reporter Occupation
- UNKNOWN
Narratives
Additional Manufacturer Narrative · 1
MINDRAY SERVICE REP REPLACED THE GAS BENCH AND VERIFIED OPERATION.
Description of Event or Problem · 1
CUSTOMER REPORTED AN ISSUE WITH THE O2 MONITORING ON THE GAS MODULE III. NO PATIENT INJURY WAS REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 187808 | GAS MODULE III RESPIRATION GAS MONITOR | GAS MODULE | BZK | MINDRAY DS USA, INC. |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |