Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Reprocessed Electrophysiology Catheter Cables Catalog Number: CB3434CT Recalled by Stryker Sustainability Solutions Due to A breach in the sterile packaging may have...
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 Electrophysiology Catheter Cables Catalog Number: CB3434CT, D134401, CB3410CT, CB3412CT Electrophysiology catheter cables are designed as electrode cables with a multi-pin connector on the distal end and the appropriate number of tails on the proximal end. The cables either interface an EP catheter with the appropriate external stimulation or recording equipment or, serve as an extension cable between an EP catheter and equipment out of immediate reach
Why Was This Recalled?
A breach in the sterile packaging may have occurred resulting in potentially non-sterile product.
Where Was This Sold?
This product was distributed to 35 states: AL, AK, AZ, CA, CO, CT, DE, FL, GA, IN, IA, KS, MD, MI, MN, MS, MT, NV, NH, NJ, NM, NY, NC, OH, OK, OR, PA, SC, SD, TN, TX, VA, WA, WI, DC
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