FDA Adverse Event Malfunction Summary report: N

TRANSTAR STRETCHER

MDR report key: 2934889 · Received December 21, 2012

Report

Report Number
1824206-2012-08485
Event Type
Malfunction
Date Received
December 21, 2012
Date of Event
December 4, 2012
Report Date
December 4, 2012
Manufacturer
HILL-ROM, INC.
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN ISOLATED THE ISSUE TO THE RATCHET RIVETS MISSING FROM THE TOP RAIL TUBES; HE REPLACED THE SIX RATCHET RIVETS TO REPAIR THE BED.

Description of Event or Problem · 1

INFORMATION RECEIVED INDICATES THE SIDERAIL IS NOT STAYING UP.

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