FDA Adverse Event
Malfunction
Summary report: N
GOBED II
MDR report key: 2223146
·
Received August 16, 2011
Report
- Report Number
- 1831750-2011-08712
- Event Type
- Malfunction
- Date Received
- August 16, 2011
- Date of Event
- July 19, 2011
- Report Date
- July 19, 2011
- Manufacturer
- STRYKER MEDICAL
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- GA, US
- Reporter Occupation
- UNKNOWN
Narratives
Additional Manufacturer Narrative · 1
LIQUID SHORTED OUT FOOTBOARD CONNECTOR PREVENTING CPU FROM WORKING. FAULTY NUT IN LIFT MOTOR.
Description of Event or Problem · 1
IT WAS REPORTED BY SERVICE REPORT THAT THE BED WAS DRIFTING AND THERE WAS EVIDENCE OF FLUID INGRESS IN THE FOOTBOARD. THE CUSTOMER COULD NOT DETERMINE IF THERE WAS PATIENT INVOLVEMENT OR IF THERE WERE ADVERSE CONSEQUENCES TO REPORT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | GOBED II | A/C HOSPITAL BED | FNL | STRYKER MEDICAL | FL28EX | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNK |