FDA Adverse Event
Malfunction
Summary report: N
TRANSTAR STRETCHER
MDR report key: 2220112
·
Received August 15, 2011
Report
- Report Number
- 1824206-2011-04312
- Event Type
- Malfunction
- Date Received
- August 15, 2011
- Date of Event
- August 3, 2011
- Report Date
- August 3, 2011
- Manufacturer
- HILL-ROM, INC.
- Product Code
- FPO
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NY, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE TECH FOUND THE RIGHT SIDERAIL END TUBE WAS BROKEN. HE REPLACED THE END TUBE AND THE RIVETS TO REPAIR THE STRETCHER.
Description of Event or Problem · 1
INFO RECEIVED INDICATES THE SIDERAIL IS NOT STAYING IN THE RAISED POSITION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | TRANSTAR STRETCHER | WHEELED STRETCHER | FPO | HILL-ROM, INC. | 8000 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |