FDA Adverse Event
Malfunction
Summary report: N
OBGYN STRETCHER
MDR report key: 2243505
·
Received August 22, 2011
Report
- Report Number
- 3006697241-2011-00086
- Event Type
- Malfunction
- Date Received
- August 22, 2011
- Date of Event
- August 12, 2011
- Report Date
- August 12, 2011
- Manufacturer
- HILL-ROM DE MEXICO S DE RL DE CV
- Product Code
- FPO
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NY, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE TECH ISOLATED THE ISSUE TO THE GAS SPRINGS. HE REPLACED THE GAS SPRINGS TO REPAIR THE STRETCHER.
Description of Event or Problem · 1
INFO RECEIVED INDICATES THE HEAD SECTION IS STUCK IN THE RAISED POSITION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | OBGYN STRETCHER | WHEELED STRETCHER | FPO | HILL-ROM DE MEXICO S DE RL DE CV | 8050 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |