FDA Adverse Event
Malfunction
Summary report: N
SECURE II MED/SURG BED
MDR report key: 1800610
·
Received August 3, 2010
Report
- Report Number
- 1831750-2010-01701
- Event Type
- Malfunction
- Date Received
- August 3, 2010
- Date of Event
- July 8, 2010
- Report Date
- July 8, 2010
- Manufacturer
- STRYKER CORP, MEDICAL DIV
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FL, US
- Reporter Occupation
- UNKNOWN
Narratives
Description of Event or Problem · 1
IT WAS REPORTED THAT THE BED HAD A BAD COMM CORD AND A BROKEN INNER ARM COVER.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | SECURE II MED/SURG BED | AC POWERED HOSPITAL BED | FNL | STRYKER CORP, MEDICAL DIV | 3002 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA |