FDA Adverse Event Malfunction Summary report: N

VERSACARE BED

MDR report key: 3071018 · Received April 8, 2013

Report

Report Number
1824206-2013-01991
Event Type
Malfunction
Date Received
April 8, 2013
Date of Event
March 13, 2013
Report Date
March 13, 2013
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
KS, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

NO FURTHER INFO IS AVAILABLE ON THE REPAIR OF THE BED AT THIS TIME.

Description of Event or Problem · 1

THE ACCOUNT ALLEGED THE BED WILL NOT SEND A NURSE CALL. NO INJURY REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
144535 VERSACARE BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 3200

Patients

Seq Age Sex Outcome Treatment
1