FDA Adverse Event Malfunction Summary report: N

TOTALCARE BED

MDR report key: 3031335 · Received March 5, 2013

Report

Report Number
1824206-2013-01231
Event Type
Malfunction
Date Received
March 5, 2013
Date of Event
February 6, 2013
Report Date
February 6, 2013
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THE HILL-ROM TECH REPLACED THE HEAD UP VALVE TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

INFORMATION RECEIVED INDICATED THE HEAD SECTION WOULD NOT RAISE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
94879 TOTALCARE BED AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1900

Patients

Seq Age Sex Outcome Treatment
1