FDA Adverse Event Malfunction Summary report: N

PVC, CLEAR, CONTRAST INJECTION TUBING

MDR report key: 2093223 · Received April 14, 2011

Report

Report Number
1721504-2011-00138
Event Type
Malfunction
Date Received
April 14, 2011
Date of Event
February 25, 2011
Report Date
March 18, 2011
Manufacturer
MERIT MEDICAL SYSTEMS, INC.
Product Code
DXJ
PMA / PMN Number
K883718
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

ONE USED SUSPECT DEVICE WAS RETURNED FOR EVALUATION. UPON VISUAL INSPECTION THE COMPLAINT WAS CONFIRMED. THE ROTATOR WAS SEPARATED AT THE BOND BETWEEN THE COLLAR AND THE HOUSING. A REVIEW OF THE DEVICE HISTORY RECORD DID NOT REVEAL ANY EXCEPTION DOCUMENTS. THE COMPLAINT DATABASE WAS REVIEWED AND FOUND ONE SIMILAR COMPLAINT FOR THIS LOT NUMBER. THE CUSTOMER DID NOT PROVIDE ANY INFORMATION AS TO IF THIS WAS THE INITIAL USE OF THE DEVICE. THE ROOT CAUSES OF THE FAILURE ARE ATTRIBUTED TO THE MANUFACTURING BONDING PROCESS. CORRECTIVE ACTIONS HAVE BEEN IMPLEMENTED TO ADDRESS THIS TYPE OF FAILURE. THIS LOT WAS BUILT PRIOR TO IMPLEMENTATION OF THE NOTED CORRECTIVE ACTIONS. METHOD: DEVICE HISTORY RECORD WAS REVIEWED, COMPLAINT DATABASE WAS REVIEWED.

Description of Event or Problem · 1

THE ROTATOR BROKE DURING A LEFT VENTRICULOGRAM PROCEDURE. THE CUSTOMER REPORTED THAT THIS OCCURRED FOUR TIMES. INJECTOR SETTINGS: 10 ML/SEC FOR A TOTAL OF 30 ML AT 600 PSI. NO HARM OR INJURY WAS REPORTED. THIS IS ONE OF FOUR REPORTS FOR THIS COMPLAINT: 1721504-2011-00136, 1721504-2011-00137, 1721504-2011-00139.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PVC, CLEAR, CONTRAST INJECTION TUBING DISPLAY, CATHODE RAY-TUBE, MEDICAL DXJ MERIT MEDICAL SYSTEMS, INC. F731037

Patients

Seq Age Sex Outcome Treatment
1 4FR PIGTAIL CATHETER