FDA Adverse Event Malfunction Summary report: N

TOTALCARE SPORT

MDR report key: 2943503 · Received January 9, 2013

Report

Report Number
1824206-2013-00219
Event Type
Malfunction
Date Received
January 9, 2013
Date of Event
December 26, 2012
Report Date
December 26, 2012
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
VA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE HILL-ROM TECHNICIAN FOUND THAT THERE WAS SOME DRIED FLUID BUILT UP ON THE SIDERAIL LATCH COMPONENTS KEEPING THE SIDERAIL FROM LATCHING. HE CLEANED THE SIDERAIL LATCHING COMPONENTS TO REPAIR THE BED.

Description of Event or Problem · 1

INFO RECEIVED INDICATED THE LEFT SIDERAIL WOULD NOT LATCH.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
12872 TOTALCARE SPORT AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1900

Patients

Seq Age Sex Outcome Treatment
1