FDA Adverse Event
Malfunction
Summary report: N
ANESTHETIC GAS MODULE
MDR report key: 252589
·
Received December 1, 1999
Report
- Report Number
- 9610816-1999-00008
- Event Type
- Malfunction
- Date Received
- December 1, 1999
- Report Date
- September 17, 1999
- Manufacturer
- AGILENT TECHNOLOGIES, GMBH
- Product Code
- CBQ
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- JA
- Reporter Occupation
- PHYSICIAN
Narratives
Description of Event or Problem · 1
THE CUSTOMER REPORTED THAT THE WATERTRAP IS TOO BRITTLE IF SAMPLE TUBE IS BEING PULLED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | ANESTHETIC GAS MODULE | AGM | CBQ | AGILENT TECHNOLOGIES, GMBH | M1026A | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA |