FDA Adverse Event
Malfunction
Summary report: N
SECURE 2 MED/SURGBED
MDR report key: 2023955
·
Received March 10, 2011
Report
- Report Number
- 1831750-2011-02392
- Event Type
- Malfunction
- Date Received
- March 10, 2011
- Date of Event
- February 15, 2011
- Report Date
- February 15, 2011
- Manufacturer
- STRYKER MEDICAL
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
RESULT: FOOTBOARD.
Description of Event or Problem · 1
IT WAS REPORTED BY SERVICE REPORT THAT THE POWER CORD WAS DAMAGED WITH EXPOSED WIRES. IT WAS FURTHER REPORTED THE FOOTBOARD WAS DAMAGED WITH EXPOSED SHARP EDGES. IT IS NOT KNOWN IF THERE WAS PATIENT INVOLVEMENT OR ANY ADVERSE CONSEQUENCES.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | SECURE 2 MED/SURGBED | A/C POWERED HOSPITAL BED | FNL | STRYKER MEDICAL | 3002 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |