NeoPICC recall
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http://www.arrowintl.com/about/investor/120304.asp
For Immediate Release
Date: December 3, 2004 Media Contact:
Frederick J. Hirt, 610-478-3117
ARROW INTERNATIONAL ISSUES NATIONWIDE VOLUNTARY RECALL OF
NeoPICC® 1.9 FR PERIPHERALLY INSERTED CENTRAL CATHETER
READING, PA, December 3, 2004 - Arrow International, Inc., today announced that after consulting with the FDA, the Company is voluntarily initiating a nationwide recall of all of the NeoPICC® 1.9 FR Peripherally Inserted Central Catheters (Product Numbers S1PIC19-N; S1PIC19-S; S1PIC19-SMK; and S1PIC19-C).
Arrow International is reviewing reports and investigating the root cause of several adverse events during which the NeoPICC® 1.9 FR Peripherally Inserted Central Catheter was utilized. These events, including one death, have been reported to involve possible vessel erosion.
Medical professionals who have NeoPICC® 1.9 FR Peripherally Inserted Central Catheters are advised to cease using the device. The devices can be identified by their product number.
NeoPICC® 1.9 FR Peripherally Inserted Central Catheters are distributed nationwide through the Company's distributors and to hospitals. Arrow distributes approximately 65,000 units of these products annually.
On November 23, 2004, Arrow International issued a Field Notification to its distributors and customers and is arranging for the return of all NeoPICC® 1.9 FR Peripherally Inserted Central Catheters.
Medical professionals with questions may contact Arrow Customer Service 24 hours a day, toll free, at 1-800-523-8446.
Do any of you use these and what are you doing with the babies that have these lines already in?
The events that have happened are already risks from using a PICC. We are giving the parents the option of us pulling them and replacing it or continuing to use the line.