FDA Adverse Event
Malfunction
Summary report: N
PROCEDURAL STRETCHER
MDR report key: 3061540
·
Received March 27, 2013
Report
- Report Number
- 1824206-2013-01730
- Event Type
- Malfunction
- Date Received
- March 27, 2013
- Date of Event
- February 27, 2013
- Report Date
- February 27, 2013
- Manufacturer
- HILL-ROM, INC.
- Product Code
- FPO
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE CASTERS WERE REPLACED TO RESOLVE THE ISSUE.
Description of Event or Problem · 1
INFO RECEIVED INDICATED THE BRAKES WOULD NOT HOLD.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 124977 | PROCEDURAL STRETCHER | WHEELED STRETCHER | FPO | HILL-ROM, INC. | 800 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |