Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
ANGIOGUARD RX / XP Emboli Capture Guidewire System Recalled by Cordis US Corp Due to There is a potential for separation of the...
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
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 401814RMC
Quantity: 283 units
Why Was This Recalled?
There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement device is prepared.
Where Was This Sold?
Worldwide distribution.
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