Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ProTrack Microcatheter. Model/Catalog Numbers CIC38-145 Recalled by Baylis Medical Corp * Due to Microcatheter may have circumferential defects (cracks) along its...
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 Baylis Medical Corp * directly.
Affected Products
ProTrack Microcatheter. Model/Catalog Numbers CIC38-145, CIC35-145. Sterile, single use device intended to be used as a standard infusion wire or as an exchange guide for exchanging guidewires. Coaxial Injectable catheter guide wire. Cardiovascular.
Quantity: 433 units
Why Was This Recalled?
Microcatheter may have circumferential defects (cracks) along its shaft.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Baylis Medical Corp *
Baylis Medical Corp * has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report