FDA Adverse Event
Malfunction
Summary report: N
1833497-2008-00001
MDR report key: 1231910
·
Received August 7, 2008
Report
- Report Number
- 1833497-2008-00001
- Event Type
- Malfunction
- Date Received
- August 7, 2008
- Product Code
- INN
- Report Source
- Manufacturer report
Narratives
Additional Manufacturer Narrative · 1
USER INSTRUCTIONS AND LABELING TELL USER FACILITIES TO ROUTINELY INSPECT CHAIRS FOR CRACKS AND DAMAGE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | INN | SC720 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |