FDA Adverse Event
Malfunction
Summary report: N
PROCEDURAL STRETCHER
MDR report key: 3130354
·
Received March 14, 2013
Report
- Report Number
- 3006697241-2013-00056
- Event Type
- Malfunction
- Date Received
- March 14, 2013
- Manufacturer
- HILL-ROM DE MEXICO
- Product Code
- FPO
- Report Source
- Manufacturer report
Narratives
Additional Manufacturer Narrative · 1
THE HYDRAULIC FOOT CYLINDER WAS REPLACED TO RESOLVE THE ISSUE.
Description of Event or Problem · 1
(B)(4).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 108512 | PROCEDURAL STRETCHER | WHEELED STRETCHER | FPO | HILL-ROM DE MEXICO |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |