FDA Adverse Event
Malfunction
Summary report: N
MEDFUSION 2001 SYRINGE INFUSION PUMP
MDR report key: 1111945
·
Received August 11, 2008
Report
- Report Number
- 2183502-2008-00216
- Event Type
- Malfunction
- Date Received
- August 11, 2008
- Date of Event
- July 17, 2008
- Report Date
- August 11, 2008
- Manufacturer
- SMITHS MEDICAL MD
- Product Code
- FRN
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- ND, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
DEVICE EVALUATION: THE SUSPECT DEVICE WAS RETURNED AND EVALUATED. THE AUDIBLE ALARM SPEAKER WAS FOUND TO BE WORKING BUT SOUNDED BAD AND WAS REPLACED. THIS IS BEING MONITORED FOR TRENDS.
Description of Event or Problem · 1
THE REPORTER STATED THAT THE DEVICE ALARMS TOO QUITE. THERE WAS NO PT INJURY OR TREATMENT ASSOCIATED WITH THIS EVENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | MEDFUSION 2001 SYRINGE INFUSION PUMP | SYRINGE INFUSION PUMP | FRN | SMITHS MEDICAL MD | 2001 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |