FDA Adverse Event
Injury
Summary report: N
2250051-2009-00059
MDR report key: 1325337
·
Received February 12, 2009
Report
- Report Number
- 2250051-2009-00059
- Event Type
- Injury
- Date Received
- February 12, 2009
- Product Code
- JTC
- Report Source
- Manufacturer report
Narratives
Additional Manufacturer Narrative · 1
CUSTOMER DID NOT REQUEST SVC ACTIVITY. CUSTOMER TECHNICAL SVS 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 |