FDA Adverse Event Injury Summary report: N

TOTALCARE BED

MDR report key: 2782058 · Received September 28, 2012

Report

Report Number
1824206-2012-05954
Event Type
Injury
Date Received
September 28, 2012
Date of Event
September 11, 2012
Report Date
September 12, 2012
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE HILL-ROM TECHNICIAN FOUND THAT THE HYDRAULIC MANIFOLD WAS CONTAMINATED. HE FOUND THAT SOMETIMES THE HEAD UP FUNCTION WORKED AND OTHER TIMES IT DID NOT WORK. HE REPLACED THE HYDRAULIC MANIFOLD AND THE BED FUNCTIONED TO DESIGN SPECIFICATIONS.

Description of Event or Problem · 1

INFO RECEIVED INDICATED THE HEAD SECTION WAS OPERATING INTERMITTENTLY.

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