FDA Adverse Event Malfunction Summary report: N

TOTALCARE BED

MDR report key: 2863280 · Received November 1, 2012

Report

Report Number
1824206-2012-07005
Event Type
Malfunction
Date Received
November 1, 2012
Date of Event
March 7, 2012
Report Date
March 7, 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 TECHNICIAN ISOLATED THE ISSUE TO A SUBSTANCE IN THE LATCH MECHANISM, CAUSING IT TO STICK OPEN. THE TECH CLEANED THE SIDERAIL LATCH MECHANISM TO REPAIR THE BED.

Description of Event or Problem · 1

INFO RECEIVED INDICATES THE RIGHT INTERMEDIATE SIDERAIL WILL NOT LATCH.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1