FDA Adverse Event
Malfunction
Summary report: N
STANDARD STRETCHER
MDR report key: 3162315
·
Received May 23, 2013
Report
- Report Number
- 3006697241-2013-00116
- Event Type
- Malfunction
- Date Received
- May 23, 2013
- Manufacturer
- HILL-ROM DE MEXICO S DE RL DE CV
- Product Code
- FPO
- Report Source
- Manufacturer report
Narratives
Additional Manufacturer Narrative · 1
THE ACCOUNT REPLACED THE SIDE RAIL ASSEMBLY TO RESOLVE THE ISSUE.
Description of Event or Problem · 1
(B)(4).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 228087 | STANDARD STRETCHER | WHEELED STRETCHER | FPO | HILL-ROM DE MEXICO S DE RL DE CV |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |