FDA Adverse Event
Malfunction
Summary report: N
3002 SECURE II
MDR report key: 2231498
·
Received July 22, 2011
Report
- Report Number
- 1831750-2011-07493
- Event Type
- Malfunction
- Date Received
- July 22, 2011
- Date of Event
- June 24, 2011
- Report Date
- June 24, 2011
- Manufacturer
- STRYKER MEDICAL
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- VA, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
RESULTS - INCORRECT BRAKE PLATE KIT INSTALLED. DAMAGED POWER CORD OUTER SHEATHING. DAMAGED MOTION INTERRUPT PAN.
Description of Event or Problem · 1
IT WAS REPORTED BY SERVICE REPORT THAT THE MOTION INTERRUPT PAN WAS CRACKED, THE POWER CORD HAD THE OUTER SHEATHING DAMAGE EXPOSED WIRES, AND THE BRAKES HAD A REDUCTION OF BRAKE FORCE. 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 |