FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 1780154 · Received May 7, 2010

Report

Report Number
1824206-2010-06976
Event Type
Malfunction
Date Received
May 7, 2010
Date of Event
April 12, 2010
Report Date
April 12, 2010
Manufacturer
HILL-ROM INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
NOT APPLICABLE

Narratives

Description of Event or Problem · 1

TECHNICIAN ALLEGED SIDERAIL WOULD NOT LATCH. HE FOUND E-RINGS MISSING ON LATCH PIN. HE REPLACED MISSING PART TO RESOLVE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTALCARE AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. P1900K006231

Patients

Seq Age Sex Outcome Treatment
1