FDA Adverse Event Injury Summary report: N

TRANSTAR STRETCHER

MDR report key: 2499616 · Received March 16, 2012

Report

Report Number
1824206-2012-01442
Event Type
Injury
Date Received
March 16, 2012
Date of Event
March 5, 2012
Report Date
March 5, 2012
Manufacturer
HILL-ROM, INC.
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
LA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

TECH FOUND THAT WHEN THE BRAKE WAS APPLIED THE CASTERS WOULD SWIVEL. REPLACED THE BRAKE CASTERS TO RESOLVE THIS ISSUE. UNIT LOCATED IN STORAGE AREA.

Description of Event or Problem · 1

INFO RECEIVED THAT WHEN THE BRAKE WAS APPLIED THE CASTERS WOULD SWIVEL. NO INJURY REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM, INC. P8000

Patients

Seq Age Sex Outcome Treatment
1