FDA Adverse Event Malfunction Summary report: N

CENTRA BED

MDR report key: 2881248 · Received November 14, 2012

Report

Report Number
1824206-2012-07440
Event Type
Malfunction
Date Received
November 14, 2012
Date of Event
October 24, 2012
Report Date
October 24, 2012
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

THE TECHNICIAN FOUND THE BRAKES WERE MISSING THE ROLL PIN. THE TECHNICIAN REPLACED THE ROLL PIN AND BRAKE CAM TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

THE TECHNICIAN ALLEGED THAT THE BRAKES ON THE BED DID NOT HOLD. NO PATIENT 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