FDA Adverse Event
Malfunction
Summary report: N
BERTEC,2000,SA W/WHEELS BED
MDR report key: 2113563
·
Received May 24, 2011
Report
- Report Number
- 1831750-2011-05007
- Event Type
- Malfunction
- Date Received
- May 24, 2011
- Date of Event
- April 26, 2011
- Report Date
- April 26, 2011
- Manufacturer
- STRYKER MEDICAL
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- AZ, US
- Reporter Occupation
- UNKNOWN
Narratives
Additional Manufacturer Narrative · 1
FAULTY LIFT MOTOR AND BROKEN SCREW NUT ON MOTOR.
Description of Event or Problem · 1
IT WAS REPORTED BY SERVICE REPORT THAT THE BED WOULD NOT RAISE OR LOWER. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | BERTEC,2000,SA W/WHEELS BED | A/C HOSPITAL BED | FNL | STRYKER MEDICAL | 32002 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNK |