FDA Adverse Event Malfunction Summary report: N

DURASTAR STRETCHER

MDR report key: 2022448 · Received February 16, 2011

Report

Report Number
1824206-2011-00911
Event Type
Malfunction
Date Received
February 16, 2011
Date of Event
January 25, 2011
Report Date
January 25, 2011
Manufacturer
HILL-ROM, INC.
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECH ADJUSTED THE CASTERS TO REPAIR THE STRETCHER.

Description of Event or Problem · 1

INFO RECEIVED INDICATES ONE OF THE CASTERS WILL ROLL WHEN LOCKED IN BRAKE. THE CASTER WOULD UNLOCK AS SOON AS THE STRETCHER WAS PULLED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 DURASTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM, INC. 8005

Patients

Seq Age Sex Outcome Treatment
1