FDA Adverse Event
Malfunction
Summary report: N
SECURE II MED/SURG BED
MDR report key: 1993341
·
Received January 21, 2011
Report
- Report Number
- 1831750-2011-00746
- Event Type
- Malfunction
- Date Received
- January 21, 2011
- Date of Event
- December 9, 2010
- Report Date
- December 9, 2010
- Manufacturer
- STRYKER CORP., MEDICAL DIVISION
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IL, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
IT WAS REPORTED BY SERVICE REPORT THAT THE POWER CORD WAS MISSING ITS GROUND PRONG. IT IS UNK IF THERE WAS PT INVOLVEMENT OR IF THERE ARE ADVERSE CONSEQUENCES TO REPORT.
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 DIVISION | 3002 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |