FDA Adverse Event
Malfunction
Summary report: N
SECURE II MED/SURG BED
MDR report key: 2010189
·
Received March 1, 2011
Report
- Report Number
- 1831750-2011-02011
- Event Type
- Malfunction
- Date Received
- March 1, 2011
- Date of Event
- January 31, 2011
- Report Date
- January 31, 2011
- Manufacturer
- STRYKER MEDICAL
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MA, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
RESULT: MOTION INTERRUPT PAN. NO BED EXIT ISSUE WAS FOUND.
Description of Event or Problem · 1
IT WAS REPORTED BY SERVICE REPORT THAT THE UNIT IS HAVING BED EXIT ISSUE. IT WAS FURTHER REPORTED THE MOTION INTERRUPT PAN WAS MISSING. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | SECURE II MED/SURG BED | A/C POWERED HOSPITAL BED | FNL | STRYKER MEDICAL | 3002 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |