FDA Adverse Event Malfunction Summary report: N

TRANSTAR STRETCHER

MDR report key: 1052202 · Received May 21, 2008

Report

Report Number
1824206-2008-02574
Event Type
Malfunction
Date Received
May 21, 2008
Date of Event
April 23, 2008
Report Date
April 23, 2008
Manufacturer
HILL-ROM RITTER
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TN, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

UPON COMPLAINT REVIEW, IT WAS DETERMINED THAT THE REOCCURRENCE OF THIS MALFUNCTION COULD POTENTIALLY CAUSE SERIOUS INJURY AND IS THEREFORE BEING REPORTED. THE TECHNICIAN DID NOT FIND ANY SHARP EDGES BUT FILED AND ROUNDED ALL EDGES TO RESOLVE ANY FURTHER PROBLEMS.

Description of Event or Problem · 1

AN ACCOUNT REPORTED THAT WHILE USING A GAS DELIVERY ACCESSORY ON THIS STRETCHER THAT SEVERAL STAFF MEMBERS RECEIVED ABRASIONS DUE TO A SHARP EDGE ON A PORTION OF THE ACCESSORY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM RITTER P8010 NA

Patients

Seq Age Sex Outcome Treatment
1