FDA Adverse Event
Malfunction
Summary report: N
ELECTRIC MED/SURG BED
MDR report key: 2133189
·
Received May 4, 2011
Report
- Report Number
- 1831750-2011-04311
- Event Type
- Malfunction
- Date Received
- May 4, 2011
- Date of Event
- April 8, 2011
- Report Date
- April 8, 2011
- Manufacturer
- STRYKER MEDICAL
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- UNKNOWN
Narratives
Additional Manufacturer Narrative · 1
RESULTS - EXPOSED WIRES FROM A DAMAGED POWER INLET FILTER.
Description of Event or Problem · 1
IT WAS REPORTED BY SERVICE REPORT THAT THE POWER INLET WAS DAMAGED ON THE MAIN POWER CORD. IT IS UNKNOWN IF THERE WAS PATIENT INVOLVEMENT, HOWEVER NO ADVERSE CONSEQUENCES ARE REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | ELECTRIC MED/SURG BED | A/C HOSPITAL BED | FNL | STRYKER MEDICAL | FL23E | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNK |