FDA Adverse Event Malfunction Summary report: N

VERSACARE BED

MDR report key: 2172453 · Received June 17, 2011

Report

Report Number
1824206-2011-03299
Event Type
Malfunction
Date Received
June 17, 2011
Date of Event
May 27, 2011
Report Date
May 27, 2011
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN REPLACED THE INLINE SPRINGS ON ALL FOUR SIDERAILS TO REPAIR THE BED.

Description of Event or Problem · 1

INFO RECEIVED INDICATES THE SIDERAIL ARE NOT LATCHING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 VERSACARE BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 3200

Patients

Seq Age Sex Outcome Treatment
1