FDA Adverse Event
Malfunction
Summary report: N
DURASTAR STRETCHER
MDR report key: 2020493
·
Received February 16, 2011
Report
- Report Number
- 1824206-2011-00910
- Event Type
- Malfunction
- Date Received
- February 16, 2011
- Date of Event
- January 25, 2011
- Report Date
- January 25, 2011
- 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 TECHNICIAN FOUND THE RATCHET RIVETS WERE MISSING FORM THE SIDERAIL. HE REPLACED THE HARDWARE AND ADDED A ZERO TRANSFER GAP STOP TO REPAIR THE STRETCHER.
Description of Event or Problem · 1
INFORMATION RECEIVED INDICATES THE SIDERAIL FLARES OUT TO THE SIDE AND WILL NOT LOCK IN THE UPRIGHT POSITION.
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 |