FDA Adverse Event Malfunction Summary report: N

VERSACARE BED

MDR report key: 3240045 · Received July 11, 2013

Report

Report Number
1824206-2013-03469
Event Type
Malfunction
Date Received
July 11, 2013
Date of Event
June 17, 2013
Report Date
June 17, 2013
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 FOUND THE BED EXIT FUNCTIONED AS DESIGNED. NO REPAIR NEEDED.

Description of Event or Problem · 1

THE ACCOUNT ALLEGED THE BED EXIT WAS NOT FUNCTIONING. NO PATIENT IMPACT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
321413 VERSACARE BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. 3200

Patients

Seq Age Sex Outcome Treatment
1