FDA Adverse Event
Other
Summary report: N
1218813-2006-00001
MDR report key: 787794
·
Received November 2, 2006
Report
- Report Number
- 1218813-2006-00001
- Event Type
- Other
- Date Received
- November 2, 2006
- Product Code
- HQJ
- Report Source
- Manufacturer report
Narratives
Additional Manufacturer Narrative · 1
CONTACTED ST. LUKE'S BY TELEPHONE ON TWO OCCASIONS, AND CALLS WERE RETURNED. SENT A CERTIFIED LETTER REQUESTING INFO WITH REGARDS TO THE PT. HAVE NOT HEARD FROM THEM TO DATE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | HQJ |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |