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FDA Issues Recall for Twin-Pass Dual Access Catheters

Oct. 7, 2016

The FDA has issued a recall of Vascular Solutions’ Twin-Pass Dual Access catheters due to potential for excess manufacturing material to remain at either end of the catheter.

The recalled products were manufactured from October 2014 to August 2016 and distributed from October 2014 to September 2016.

The recalled products are all unexpired lots of Model Numbers 5200, 5210, and 5230. — Cynthia Jessup

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