FDA Adverse Event
Malfunction
Summary report: N
GOBED II MED/SURG BED
MDR report key: 2222078
·
Received August 16, 2011
Report
- Report Number
- 1831750-2011-08722
- Event Type
- Malfunction
- Date Received
- August 16, 2011
- Date of Event
- July 20, 2011
- Report Date
- July 20, 2011
- Manufacturer
- STRYKER MEDICAL
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MO, US
- Reporter Occupation
- UNKNOWN
Narratives
Additional Manufacturer Narrative · 1
DAMAGED SIDERAIL CABLE, FAULTY NUT IN LIFT MOTOR.
Description of Event or Problem · 1
IT WAS REPORTED BY SERVICE REPORT THAT THE BED LIFT IS DRIFTING DOWN AND THERE WAS UNINTENDED MOTION. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | GOBED II MED/SURG BED | A/C HOSPITAL BED | FNL | STRYKER MEDICAL | FL25C | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNK |