FDA Adverse Event Malfunction Summary report: N

TRANSTAR STRETCHER

MDR report key: 2020080 · Received March 10, 2011

Report

Report Number
1824206-2011-01414
Event Type
Malfunction
Date Received
March 10, 2011
Date of Event
February 14, 2011
Report Date
February 14, 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 CASTERS WERE WORN. HE REPLACED THE FOOT END CASTERS TO REPAIR THE STRETCHER.

Description of Event or Problem · 1

INFORMATION RECEIVED INDICATES THE FOOT END CASTERS ARE RATCHETING IN BRAKE WHEN PRESSURE IS APPLIED TO THE SIDE OF THE STRETCHER.

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