FDA Adverse Event Malfunction Summary report: N

DURASTAR STRETCHER

MDR report key: 2012908 · Received March 4, 2011

Report

Report Number
1824206-2011-01268
Event Type
Malfunction
Date Received
March 4, 2011
Date of Event
February 10, 2011
Report Date
February 10, 2011
Manufacturer
HILL-ROM, INC.
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN FOUND THE HEAD END BRAKE CASTERS WERE SWIVELING WHEN IN BRAKE. HE REPLACED THE HEAD END CASTERS TO REPAIR THE STRETCHER.

Description of Event or Problem · 1

THE HEAD END OF THE STRETCHER MOVES A LITTLE FROM SIDE TO SIDE WHILE IN BRAKE.

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