FDA Adverse Event
Death
Summary report: N
1931947-2006-00001
MDR report key: 956587
·
Received November 28, 2007
Report
- Report Number
- 1931947-2006-00001
- Event Type
- Death
- Date Received
- November 28, 2007
- Product Code
- FNL
- Report Source
- Manufacturer report
Narratives
Additional Manufacturer Narrative · 1
PER TELEPHONE CONVERSATION DATED 7/17/06 BETWEEN USER FACILITY STAFF: FACILITY MGR, HEAD NURSE, RISK MGR AND NOA MEDICAL INDUSTRIES PERSONNEL: ENGINEERING MGR, CONTRACT ENGINEER. FACILITY MANAGER STATED THEIR INVESTIGATION DETERMINED THAT THERE WAS NO DEFECT/MALFUNCTION OF THE BED OR SIDE RAILS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | FNL |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |