FDA Adverse Event
Malfunction
Summary report: N
OBGYN TRANSTAR STRETCHER
MDR report key: 2020087
·
Received March 10, 2011
Report
- Report Number
- 1824206-2011-01410
- Event Type
- Malfunction
- Date Received
- March 10, 2011
- Date of Event
- February 14, 2011
- Report Date
- February 14, 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 TECHNICIAN UPGRADED THE BRAKE LINKAGE TO REPAIR THE STRETCHER.
Description of Event or Problem · 1
INFORMATION RECEIVED INDICATES THE STRETCHER STILL ROLLS AFTER THE BRAKE/STEER PEDAL IS PLACED INTO THE BRAKE POSITION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | OBGYN TRANSTAR STRETCHER | WHEELED STRETCHER | FPO | HILL-ROM, INC. | 8050 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |