FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 1872685 · Received October 8, 2010

Report

Report Number
1824206-2010-10393
Event Type
Malfunction
Date Received
October 8, 2010
Date of Event
September 15, 2010
Report Date
September 15, 2010
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MO, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THE TECH REPLACED THE SIDERAIL LATCHES TO REPAIR THE BED.

Description of Event or Problem · 1

INFO RECEIVED INDICATES ALL FOUR SIDERAILS WILL NOT LATCH ON THE BED. BED WAS IN THE MAINTENANCE SHOP.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1