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FDA labels recall of Teleflex unit's catheters as Class I
6/26/2017

A recall initiated by Teleflex covering 4,679 units of Venture surgical catheters, manufactured by its subsidiary Vascular Solutions, has been classified by the FDA as Class I. The recall was issued because of a risk of embolism, which could happen if an excess material within the catheter separates during use and enters the body.

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