FDA Adverse Event Malfunction Summary report: N

TRANSTART STRETCHER

MDR report key: 3073035 · Received April 6, 2013

Report

Report Number
1824206-2013-01962
Event Type
Malfunction
Date Received
April 6, 2013
Date of Event
March 8, 2013
Report Date
March 8, 2013
Manufacturer
HILL-ROM, INC.
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE ACCOUNT REPLACED THE BRAKE CASTERS TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

THE ACCOUNT ALLEGED THE BRAKE CASTERS ROTATE TO THE SIDE WHEN THE BRAKE IS SET AND THE BED IS PUSHED. NO INJURY REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
142420 TRANSTART STRETCHER WHEELED STRETCHER FPO HILL-ROM, INC. 8040

Patients

Seq Age Sex Outcome Treatment
1