FDA Adverse Event Malfunction Summary report: N

CENTRA BED

MDR report key: 1960135 · Received December 17, 2010

Report

Report Number
1824206-2010-11699
Event Type
Malfunction
Date Received
December 17, 2010
Date of Event
November 29, 2010
Report Date
November 29, 2010
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

TECH FOUND THAT THE BED EXIT TAPE STRIP IS BAD. TECH REPLACED THE BED EXIT TAPE STRIP TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

TECH ALLEGED THAT THE BED EXIT WAS NOT ALARMING WHEN ACTIVATED. NO PT IMPACT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CENTRA BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 850

Patients

Seq Age Sex Outcome Treatment
1