Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

Cordis Vista Brite Tip & Androit Guiding Catheters Product Usage: Recalled by Cordis Corporation Due to Frayed pieces of the mounting card being inside...

Date: February 7, 2019
Company: Cordis Corporation
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Cordis Corporation directly.

Affected Products

Cordis Vista Brite Tip & Androit Guiding Catheters Product Usage: The guiding catheter is intended for use for intravascular introduction of interventional/diagnostic devices into the coronary or peripheral vascular systems.

Quantity: 23481

Why Was This Recalled?

Frayed pieces of the mounting card being inside the primary packaging.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Cordis Corporation

Cordis Corporation has 39 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report