Cordis Corporation: Medical Device Recalls in 2016

Updated on March 25, 2026.

According to to data from the FDA, there were 3 medical device recalls made by Cordis Corporation in 2016. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

Cordis PRECISE (R) PRO RX Nitinol Stent System (Carotid)
Cordis PRECISE (R) RX Nitinol Stent System (Biliary)
CORDIS AVANTI + CATHETER SHEATH INTRODUCER SYSTEM The product includes a Catheter Sheath Introducer (CSI) and a vessel dilator. A Catheter Sheath Introducer facilitates percutaneous entry of an intravascular device. A vessel dilator facilitates the percutaneous entry of the CSI by forming an atraumatic transition from the skin through the subcutaneous tissue to the vessel.