FDA Adverse Event
Other
Summary report: N
SECURE 3 MED/SURG BED
MDR report key: 1920580
·
Received December 7, 2010
Report
- Report Number
- 1831750-2010-04590
- Event Type
- Other
- Date Received
- December 7, 2010
- Date of Event
- November 8, 2010
- Report Date
- November 8, 2010
- Manufacturer
- STRYKER CORP., MEDICAL DIVISION
- Product Code
- FNL
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- ME, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
CONCLUSION: DIP SWITCH SETTINGS RECONFIGURED.
Description of Event or Problem · 1
IT WAS REPORTED BY SERVICE REPORT THAT THE NURSE CALL IS NOT FUNCTIONING. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | SECURE 3 MED/SURG BED | A/C POWERED HOSPITAL BED | FNL | STRYKER CORP., MEDICAL DIVISION | 3002S3 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |