FDA Adverse Event Malfunction Summary report: N

CENTRA

MDR report key: 1780353 · Received May 7, 2010

Report

Report Number
1824206-2010-07001
Event Type
Malfunction
Date Received
May 7, 2010
Date of Event
March 4, 2010
Report Date
March 4, 2010
Manufacturer
HILL-ROM INC.
Product Code
FNL
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

TECHNICIAN FOUND HI/LOW DRIVE DRIFTS DOWN. THE BRAKE ASSEMBLY WAS SLIPPING. HE REPLACED BRAKE ASSEMBLY PARTS TO RESOLVE.

Description of Event or Problem · 1

ACCOUNT STATED THE BED NEEDED REPAIR.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CENTRA AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. P850

Patients

Seq Age Sex Outcome Treatment
1