FDA Adverse Event
Malfunction
Summary report: N
EPICLL/ZOOM IN SERVICEVI DEO
MDR report key: 2920082
·
Received January 17, 2013
Report
- Report Number
- 0001831750-2013-00162
- Event Type
- Malfunction
- Date Received
- January 17, 2013
- Date of Event
- December 26, 2012
- Report Date
- December 26, 2012
- Manufacturer
- STRYKER MEDICAL-KALAMAZOO
- Product Code
- HDD
- PMA / PMN Number
- K960889
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MI, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
IT WAS REPORTED BY SERVICE REPORT THAT THE BED CANNOT BE LOWERED TO MINUMUM HEIGHT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 26551 | EPICLL/ZOOM IN SERVICEVI DEO | TABLE, OBSTETRICAL, AC-POWERED (AND ACCESSORIES) | HDD | STRYKER MEDICAL-KALAMAZOO |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |