FDA Adverse Event
Other
Summary report: N
SECURE II MED/SURG BED
MDR report key: 2418275
·
Received January 5, 2012
Report
- Report Number
- 1831750-2012-00094
- Event Type
- Other
- Date Received
- January 5, 2012
- Date of Event
- December 7, 2011
- Report Date
- December 7, 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
RESULT AND CONCLUSION: INCORRECT FOOTBOARD WAS INSTALLED ON BED; CORRECT FOOTBOARD INSTALLED AND BED EXIT WORKED AS SPECIFIED.
Description of Event or Problem · 1
IT WAS REPORTED BY SERVICE REPORT THAT THE BED EXIT WAS NOT WORKING. THE CUSTOMER REPORTED THAT THEY DID NOT KNOW IF THERE WAS PATIENT INVOLVEMENT OR IF THERE WERE ADVERSE CONSEQUENCES TO REPORT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | SECURE II MED/SURG BED | A/C POWERED HOSPITAL BED | FNL | STRYKER MEDICAL | 3002 EX | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |