Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
NEUROPATH 5Fx90 GUIDING CATH ST Product Code: GST50900000 Intended for Recalled by Codman & Shurtleff, Inc. Due to Sterility of device may be compromised due to...
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 Codman & Shurtleff, Inc. directly.
Affected Products
NEUROPATH 5Fx90 GUIDING CATH ST Product Code: GST50900000 Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices
Quantity: 46 units
Why Was This Recalled?
Sterility of device may be compromised due to lack of package integrity
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Codman & Shurtleff, Inc.
Codman & Shurtleff, Inc. has 58 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report