FDA Adverse Event Malfunction Summary report: N

RETROGUARD ARTERIAL SAFETY VALVE

MDR report key: 7064302 · Received November 28, 2017

Report

Report Number
1649914-2017-00100
Event Type
Malfunction
Date Received
November 28, 2017
Report Date
January 17, 2018
Manufacturer
QUEST MEDICAL, INC
Product Code
MJJ
PMA / PMN Number
K922356
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE DEVICE WAS NOT RETURNED FOR INVESTIGATION. A FOLLOW MEDWATCH WILL BE SUBMITTED IF ADDITIONAL INFORMATION BECOMES AVAILABLE.

Additional Manufacturer Narrative · 1

THE DEVICE WAS NOT RETURNED BUT A PICTURE OF THE DEVICE SHOWING THE ISSUE WAS SENT. REVIEW OF THE PICTURE CONFIRMED PRESENCE OF PARTICULATE MATTER. QUEST MEDICAL HAS IMPLEMENTED SEVERAL CONTROLS TO PREVENT THIS ISSUE INCLUDING MAINTENANCE OF AN ISO CLASS 8 MANUFACTURING ENVIRONMENT, EMPLOYEE GOWNING AND UNIFORM PROCEDURES, ROUTINE CLEANING, BATCH TO BATCH LINE CLEARANCE ACTIVITIES AND MANUFACTURING SURFACE CLEANING. PARTICULATE COUNT, TEMPERATURE AND HUMIDITY IN THE CLEAN ROOM IS CONSTANTLY MONITORED IN ACCORDANCE WITH INTERNAL ENVIRONMENTAL MONITORING PROCEDURES. THE ROOT CAUSE IS UNKNOWN. AS A PROACTIVE MEASURE, QUEST MEDICAL HAS INITIATED A CAPA TO FURTHER INVESTIGATE THIS ISSUE. NO FURTHER SUPPLEMENTS WILL BE SUBMITTED UNLESS NEW SIGNIFICANT FINDINGS EMERGE.

Description of Event or Problem · 1

A CUSTOMER REPORTED AN ISSUE WITH THE VALVE. THE REPORT STATES THAT WHILE PRIMING, THE MEDICAL STAFF FOUND A PARTICULATE MATTER COLORED IN BLACK IN THE VALVE. THE LENGTH OF THE PARTICULATE MATTER IS ABOUT 2MM (ABOUT 0.3MM²).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
841883 RETROGUARD ARTERIAL SAFETY VALVE CPB CHECK VALVE MJJ QUEST MEDICAL, INC 4007100 0521126S05

Patients

Seq Age Sex Outcome Treatment
1