FDA Adverse Event
Malfunction
Summary report: N
2250051-2008-00391
MDR report key: 1213623
·
Received August 1, 2008
Report
- Report Number
- 2250051-2008-00391
- Event Type
- Malfunction
- Date Received
- August 1, 2008
- Product Code
- JTC
- Report Source
- Manufacturer report
Narratives
Additional Manufacturer Narrative · 1
CUSTOMER DID NOT REQUEST SERVICE ACTIVITY. CUSTOMER TECHNICAL SERVICES REVIEWED THE CUSTOMER'S DATA FILES. INVESTIGATION INDICATES THAT THE CUSTOMER IS NOT USING AN OPTIMAL BARCODE SYMBOLOGY AND SYSTEM SETTING. THE CUSTOMER HAS BEEN INFORMED OF THE RESULTS OF THE INVESTIGATION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | JTC |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |