FDA Adverse Event Malfunction Summary report: N

TOTALCARE BED

MDR report key: 3192322 · Received May 29, 2013

Report

Report Number
1824206-2013-02878
Event Type
Malfunction
Date Received
May 29, 2013
Date of Event
May 1, 2013
Report Date
May 1, 2013
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECH FOUND THE SIDE RAIL LATCH ASSEMBLY IS DIRTY PREVENTING PROPER CONNECTION TO LATCH THE SIDE RAIL. THE TECH THOROUGHLY CLEANED THE SIDE RAIL LATCH ASSEMBLY TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

THE TECH ALLEGED THAT THE SIDE RAIL WILL NOT LATCH. NO PT IMPACT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
236974 TOTALCARE BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1900

Patients

Seq Age Sex Outcome Treatment
1