FDA Adverse Event
Malfunction
Summary report: N
3002 SECURE II
MDR report key: 2223352
·
Received August 17, 2011
Report
- Report Number
- 1831750-2011-08745
- Event Type
- Malfunction
- Date Received
- August 17, 2011
- Date of Event
- July 21, 2011
- Report Date
- July 21, 2011
- Manufacturer
- STRYKER MEDICAL
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- SC, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
RESULT: BOTH HEAD-END SIDERAIL PANELS WERE DAMAGED. DAMAGED POWER CORD SHEATHING. DAMAGED SIDERAIL CABLES.
Description of Event or Problem · 1
IT WAS REPORTED BY SERVICE REPORT THAT BOTH HEAD-END SIDERAIL PANELS WERE DAMAGED, AND WAS NOT FUNCTIONING, BUT WITH NO SHARP EDGES EXPOSED; THE MANUAL CPR RELEASE WAS BENT AND NOT FUNCTIONING; THE POWER CORD HAD A CUT, BUT NO EXPOSED WIRES. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | 3002 SECURE II | A/C POWERED HOSPITAL BED | FNL | STRYKER MEDICAL | 3002 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |