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Cordis Corporation recalls Cordis PRECISE (R) PRO RX Nitinol Stent System (Carotid)
Recalled June 22, 2016 · FDA recall Z-1946-2016 · Cordis
Hazard
Inability to deploy the stent or partial stent deployment. · FDA Class II
Units
4,400 units in US and 3,100 units in Foreign Countries
Sold at
NATIONWIDE and FOREIGN CONSIGNEES: Japan, Taiwan, Thailand and South Korea.
Description
Inability to deploy the stent or partial stent deployment.
Product
Cordis PRECISE (R) PRO RX Nitinol Stent System (Carotid)
Manufacturer(s)
Cordis Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →