FDA Adverse Event Injury Summary report: N

PERFORMA DIANGONSTIC CARDIOLOGY CATHETER

MDR report key: 3190149 · Received June 21, 2013

Report

Report Number
1628221-2013-00012
Event Type
Injury
Date Received
June 21, 2013
Date of Event
February 1, 2013
Report Date
May 28, 2013
Manufacturer
MERIT MEDICAL SYSTEMS, INC.
Product Code
DQO
PMA / PMN Number
K943739
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JO
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

DEVICE EVALUATION. THE SUSPECT DEVICE IS NOT EXPECTED TO BE RETURNED FOR EVALUATION. A REVIEW OF THE DEVICE HISTORY RECORD COULD NOT BE PERFORMED AS THE USER DID NOT PROVIDE A LOT NUMBER. A GENERAL REVIEW OF THE COMPLAINT DATABASE FROM 01/2010 TO 06/2013 REVEALED TWO SIMILAR COMPLAINTS FROM THE SAME USER. NO SIMILAR COMPLAINTS HAVE BEEN REPORTED FROM ANY OTHER USER. MERIT IS UNABLE TO DETERMINE THE EXACT ROOT CAUSE OF THE REPORTED FAILURE WITHOUT THE SUSPECT DEVICE. A FOLLOW-UP REPORT WILL BE SUBMITTED IF MORE INFO BECOMES AVAILABLE.

Description of Event or Problem · 1

THE USER REPORTED THAT DURING A CORONARY ANGIOGRAM PROCEDURE THE CATHETER CAUSED A DISSECTION OF THE RIGHT CORONARY ARTERY. THE USER REPORTED THAT THE PROCEDURE TOOK PLACE SOMETIME IN (B)(6) 2013. THE DATE OF EVENT PROVIDED IN THIS REPORT IS AN ESTIMATE. THE PHYSICIAN DEPLOYED A STENT TO TREAT THE DISSECTION. THE PT WAS THEN TRANSFERRED TO THE CARDIAC CARE UNIT FOR OBSERVATION AFTER WHICH THE PT WAS DISCHARGED FROM THE HOSPITAL. THE USER DID NOT PROVIDED A CATALOG ITEM NUMBER OR LOT NUMBER FOR THE CATHETER USED AND DISCARDED THE SUSPECT DEVICE AT THE HOSPITAL. HOWEVER, SHIPPING HISTORY RECORDS INDICATE THAT THE USER WAS ONLY SENT (B)(4) CATHETERS THAT CONFORMED TO THE COMPLAINT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
283123 PERFORMA DIANGONSTIC CARDIOLOGY CATHETER CATHETER, INTRAVASCULAR, DIAGNOSTIC DQO MERIT MEDICAL SYSTEMS, INC.

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization| L| R MANIFOLD - SYRINGE| CONTRAST MEDIA - SALINE