FDA Adverse Event Malfunction Summary report: N

VERSACARE

MDR report key: 1143268 · Received September 3, 2008

Report

Report Number
1824206-2008-02179
Event Type
Malfunction
Date Received
September 3, 2008
Date of Event
November 3, 2006
Report Date
November 3, 2006
Manufacturer
HILL-ROM RITTER
Product Code
FNL
Removal / Correction Number
Z-0240-2008
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

TECH - SIDERAIL WILL NOT LATCH, REPLACED WITH SIDERAIL INLINE SPRING UPGRADE KIT. BED OK.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 VERSACARE AC POWERED HOSPITAL BED FNL HILL-ROM RITTER P3200 NA

Patients

Seq Age Sex Outcome Treatment
1