FDA Adverse Event Malfunction Summary report: N

CENTRA BED

MDR report key: 3023303 · Received February 28, 2013

Report

Report Number
1824206-2013-01152
Event Type
Malfunction
Date Received
February 28, 2013
Date of Event
February 1, 2013
Report Date
February 1, 2013
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECH REPLACED THE POWER CORD PLUG TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

THE TECH ALLEGED THAT THE BED HAD A HIGH GROUND READING. NO PT IMPACT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
88965 CENTRA BED A/C POWERED ADJSUTABLE HOSPITAL BED FNL HILL-ROM, INC. 852

Patients

Seq Age Sex Outcome Treatment
1