Recall Z-1826-2017— Cordis Corporation

Name: FDA recall Z-1826-2017
Creator: U.S. Food and Drug Administration
Published: 2017-02-16

Class II · Terminated

Class II FDA medical device recall by Cordis Corporation, initiated 2017-02-16, terminated 2019-08-06. FDA's recall record names no specific 510(k) clearance for this event. Product: Cordis S.M.A.R.T. Flex Vascular Stent System. Reason: Deployment Difficulty..

Recalling firm: Cordis Corporation
Classification: Class II
Status: Terminated
Initiated: 2017-02-16
Terminated: 2019-08-06
Firm location: Miami Lakes, FL, United States

Product description

Cordis S.M.A.R.T. Flex Vascular Stent System

Reason for recall

Deployment Difficulty.

Data sourced from openFDA. This site is unofficial and independent of the FDA.