FDA Adverse Event Malfunction Summary report: N

TOTALCARE-TREAT SURFACE & SCALE

MDR report key: 1843723 · Received September 21, 2010

Report

Report Number
1824206-2010-10052
Event Type
Malfunction
Date Received
September 21, 2010
Date of Event
August 26, 2010
Report Date
August 26, 2010
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

RIGHT AND LEFT SIDERAIL LATCHES WERE BENT CAUSING THE SIDERAIL NOT TO ENGAGE IN THE LOCKING POSITION. REPLACED BOTH RIGHT AND LEFT FOOT SIDERAIL LATCHES TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

THE PT'S RIGHT AND LEFT FOOT SIDERAIL LATCH WOULD NOT ENGAGE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTALCARE-TREAT SURFACE & SCALE A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. P1900

Patients

Seq Age Sex Outcome Treatment
1