FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 1891350 · Received November 2, 2010

Report

Report Number
1824206-2010-10808
Event Type
Malfunction
Date Received
November 2, 2010
Date of Event
October 7, 2010
Report Date
October 7, 2010
Manufacturer
HILL-ROM INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TN, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN REPLACED THE LATCHES, RETAINING RINGS, SPRINGS, AND D-PINS IN BOTH SIDERAILS TO REPAIR THE BED.

Description of Event or Problem · 1

INFO RECEIVED INDICATES BOTH INTERMEDIATE SIDERAILS ARE HAVING INTERMITTENT LATCHING PROBLEMS DUE TO CORROSION ON THE LATCHES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTALCARE AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. 1900

Patients

Seq Age Sex Outcome Treatment
1 UNK