FDA Adverse Event
Malfunction
Summary report: N
DURASTAR STRETCHER
MDR report key: 2053531
·
Received March 17, 2011
Report
- Report Number
- 1824206-2011-01654
- Event Type
- Malfunction
- Date Received
- March 17, 2011
- Date of Event
- February 21, 2011
- Report Date
- February 21, 2011
- Manufacturer
- HILL-ROM, INC.
- Product Code
- FPO
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- DE, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE TECHNICIAN FOUND THE BASE OF THE END TUBE WHERE THE BOLT PASSES THROUGH WAS BROKEN OFF. THE TECHNICIAN REPLACED THE END TUBES TO REPAIR THE STRETCHER.
Description of Event or Problem · 1
INFO RECEIVED INDICATES THE SIDERAIL WILL NOT LATCH DUE TO TWO BROKEN END TUBES.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | DURASTAR STRETCHER | WHEELED STRETCHER | FPO | HILL-ROM, INC. | 8005 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |