FDA Adverse Event Malfunction Summary report: N

TRANSTAR STRETCHER

MDR report key: 2922666 · Received December 27, 2012

Report

Report Number
1824206-2012-08639
Event Type
Malfunction
Date Received
December 27, 2012
Date of Event
December 10, 2012
Report Date
December 10, 2012
Manufacturer
HILL-ROM INC.
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GA, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN REPLACED THE BRAKE CASTERS TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

THE TECHNICIAN ALLEGED THAT THE BRAKE CASTERS WILL NOT HOLD. NO PATIENT IMPACT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM INC. 8050

Patients

Seq Age Sex Outcome Treatment
1