FDA Adverse Event Malfunction Summary report: N

4 MOTOR ADVANCE BED

MDR report key: 1082763 · Received July 23, 2008

Report

Report Number
1824206-2008-02876
Event Type
Malfunction
Date Received
July 23, 2008
Date of Event
June 24, 2008
Report Date
June 24, 2008
Manufacturer
HILL-ROM RITTER
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
VA, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

REP, IN THE HOSP MAINTENANCE DEPT CALLED AND SAID THAT THE HEAD SECTION RAN UP UNINTENTIONALLY ON THIS BED. REP STATED THAT WITH THE LH HEAD SIDERAIL UNPLUGGED, THE HEAD WILL NOT RUN UP UNINTENTIONALLY. REP REPLACED THE COMPLETE SIDERAIL TO RESOLVE THE ISSUE. THERE WAS NO REPORTED INJURIES OR PT INVOLVEMENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 4 MOTOR ADVANCE BED MED SURGICAL FNL HILL-ROM RITTER 1105 NA

Patients

Seq Age Sex Outcome Treatment
1