FDA Adverse Event
Malfunction
Summary report: N
TRANSTAR STRETCHER
MDR report key: 2031716
·
Received March 21, 2011
Report
- Report Number
- 1824206-2011-01747
- Event Type
- Malfunction
- Date Received
- March 21, 2011
- Date of Event
- February 24, 2011
- Report Date
- February 24, 2011
- Manufacturer
- HILL-ROM, INC.
- Product Code
- FPO
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NC, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE TECH FOUND THE SHOULDER LATCH BOLT WAS MISSING. HE REPLACED THE BOLT TO REPAIR THE BED.
Description of Event or Problem · 1
INFO RECEIVED INDICATES THE LEFT SIDERAIL WILL NOT LATCH.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | TRANSTAR STRETCHER | WHEELED STRETCHER | FPO | HILL-ROM, INC. | 8005 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |