FDA Adverse Event
Malfunction
Summary report: N
ADEL OBS 6/04
MDR report key: 2961855
·
Received February 14, 2013
Report
- Report Number
- 0001831750-2013-01152
- Event Type
- Malfunction
- Date Received
- February 14, 2013
- Date of Event
- January 22, 2013
- Report Date
- January 22, 2013
- Manufacturer
- STRYKER MEDICAL-KALAMAZOO
- Product Code
- HDD
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TN, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
RESULT: HI / LO LIMITS NEED TO BE BURNED.
Description of Event or Problem · 1
IT WAS REPORTED BY SERVICE REPORT THAT THE BED HEAD AND FOOT SECTION WAS STUCK IN THE HIGH HEIGHT POSITION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 64732 | ADEL OBS 6/04 | TABLE, OBSTETRICAL, AC-POWERED (AND ACCESSORIES) | HDD | STRYKER MEDICAL-KALAMAZOO |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |