Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Vista Brite Tip Recalled by Cordis US Corp Due to Catheter manufactured at the incorrect length.
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 US Corp directly.
Affected Products
Vista Brite Tip, Judkins Right 4, REF SM7504, JR3 VBT (Special) 110 cm 6F. Guiding catheter is intended for use for intravascular introduction of interventional/diagnostic devices into the coronary or peripheral vascular systems.
Quantity: 12 units
Why Was This Recalled?
Catheter manufactured at the incorrect length.
Where Was This Sold?
This product was distributed to 1 state: WA
About Cordis US Corp
Cordis US Corp has 22 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report