FDA Adverse Event
Malfunction
Summary report: N
SECURE ACUTE CARE BED
MDR report key: 2231235
·
Received July 18, 2011
Report
- Report Number
- 1831750-2011-07176
- Event Type
- Malfunction
- Date Received
- July 18, 2011
- Date of Event
- June 20, 2011
- Report Date
- June 20, 2011
- Manufacturer
- STRYKER MEDICAL
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MA, US
- Reporter Occupation
- UNKNOWN
Narratives
Additional Manufacturer Narrative · 1
RESULT: MOTION INTERRUPT PAN.
Description of Event or Problem · 1
IT WAS REPORTED BY SERVICE REPORT THAT THE MOTION INTERRUPT PAN WAS HANGING ON THE HEAD LEFT SIDE OF THE BED, THE POWER CORD HAD A LOOSE PRONG, AND THE SCALE HAD AN INCORRECT WEIGHT READING. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | SECURE ACUTE CARE BED | A/C POWERED HOSPITAL BED | FNL | STRYKER MEDICAL | 3000 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |