FDA Adverse Event
Malfunction
Summary report: N
GO BED PLUS
MDR report key: 2021498
·
Received February 16, 2011
Report
- Report Number
- 1831750-2011-01491
- Event Type
- Malfunction
- Date Received
- February 16, 2011
- Date of Event
- January 21, 2011
- Report Date
- January 21, 2011
- Manufacturer
- STRYKER MEDICAL
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IA, US
- Reporter Occupation
- UNKNOWN
Narratives
Description of Event or Problem · 1
IT WAS REPORTED BY SERVICE REPORT THAT THE SIDE RAIL LOCKOUT LIGHTS ARE NOT WORKING ON THE FOOTBOARD. IT IS UNK IF THERE WAS PT INVOLVEMENT OR IF THERE ARE ADVERSE CONSEQUENCES.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | GO BED PLUS | A/C HOSPITAL BED | FNL | STRYKER MEDICAL | 2501 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNK |