Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Reprocessed Daig Supreme Fixed Curve Diagnostic Electrophysiology Catheters Recalled by Stryker Sustainability Solutions Due to Mislabeling
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 Stryker Sustainability Solutions directly.
Affected Products
Reprocessed Daig Supreme Fixed Curve Diagnostic Electrophysiology Catheters; Model #: 401450, 401877. Indicated for temporary intracardiac sensing, recording, stimulation, and electrophysiology mapping of cardiac structures.
Quantity: 18 devices
Why Was This Recalled?
Mislabeled for size
Where Was This Sold?
This product was distributed to 1 state: NY
About Stryker Sustainability Solutions
Stryker Sustainability Solutions has 38 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report