FDA Adverse Event Malfunction Summary report: N

TRANSTAR STRETCHER

MDR report key: 2011993 · Received February 14, 2011

Report

Report Number
1824206-2011-00821
Event Type
Malfunction
Date Received
February 14, 2011
Date of Event
January 20, 2011
Report Date
January 20, 2011
Manufacturer
HILL-ROM, INC.
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN FOUND THE CASTER WAS WORN. HE REPLACED THE LEFT FOOT BRAKE CASTER TO REPAIR THE BED.

Description of Event or Problem · 1

INFORMATION RECEIVED INDICATES THE LEFT FOOT BRAKE CASTER RATCHETS WHEN THE STRETCHER HAS PRESSURE APPLIED FROM SIDE AND THE BRAKE IS ENGAGED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM, INC. 8000

Patients

Seq Age Sex Outcome Treatment
1