FDA Adverse Event
Malfunction
Summary report: N
SECURE II MED/SURG BED
MDR report key: 1894617
·
Received November 5, 2010
Report
- Report Number
- 1831750-2010-03554
- Event Type
- Malfunction
- Date Received
- November 5, 2010
- Date of Event
- October 11, 2010
- Report Date
- October 11, 2010
- Manufacturer
- STRYKER CORP, MEDICAL DIV
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NY, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
TIMING LINK.
Description of Event or Problem · 1
IT WAS REPORTED BY SERVICE REPORT THAT THERE WAS NO POWER AND THE AUXILIARY POWER CORD GROUND PRONG WAS LOOSE. ADDITIONALLY, THE SIDERAIL WAS NOT FUNCTIONING. 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 CORP, MEDICAL DIV | 3002 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |