FDA Adverse Event
Malfunction
Summary report: N
TRANSTAR STRETCHER
MDR report key: 2243474
·
Received August 30, 2011
Report
- Report Number
- 3006697241-2011-00096
- Event Type
- Malfunction
- Date Received
- August 30, 2011
- Date of Event
- August 18, 2011
- Report Date
- August 18, 2011
- Manufacturer
- HILL-ROM DE MEXICO S DE RL DE CV
- Product Code
- FPO
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- VA, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE TECH FOUND THE SIDERAIL PIVOT SCREW WAS MISSING. HE INSTALLED A NEW SCREW TO REPAIR THE STRETCHER.
Description of Event or Problem · 1
INFO RECEIVED INDICATES THE SIDERAIL WILL NOT STAY UP.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | TRANSTAR STRETCHER | WHEELED STRETCHER | FPO | HILL-ROM DE MEXICO S DE RL DE CV | 8000 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |