FDA Adverse Event
Malfunction
Summary report: N
SECURE ACUTE CARE BED
MDR report key: 1760156
·
Received July 12, 2010
Report
- Report Number
- 1831750-2010-01499
- Event Type
- Malfunction
- Date Received
- July 12, 2010
- Date of Event
- June 17, 2010
- Report Date
- June 17, 2010
- Manufacturer
- STRYKER CORP., MEDICAL DIV.
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- ME, US
- Reporter Occupation
- UNKNOWN
Narratives
Additional Manufacturer Narrative · 1
SENSOR COIL CABLE.
Description of Event or Problem · 1
IT WAS REPORTED THAT THE HEAD OF THE BED WOULD ONLY LOWER HALF WAY. NO ADVERSE CONSEQUENCES WERE ALLEGED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | SECURE ACUTE CARE BED | A/C POWERED HOSPITAL BED | FNL | STRYKER CORP., MEDICAL DIV. | 3000 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA |