FDA Adverse Event Malfunction Summary report: N

TRANSTAR STRETCHER

MDR report key: 3061022 · Received March 26, 2013

Report

Report Number
1824206-2013-01673
Event Type
Malfunction
Date Received
March 26, 2013
Date of Event
February 26, 2013
Report Date
February 26, 2013
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NJ, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN REPLACED THE BRAKE CASTERS TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

THE TECHNICIAN ALLEGED THE BRAKE CASTERS ARE RATCHETING AND NOT HOLDING WHILE IN BRAKE MODE. NO PATIENT IMPACT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
123139 TRANSTAR STRETCHER A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 8000

Patients

Seq Age Sex Outcome Treatment
1