Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Custom Procedure Kit Recalled by Merit Medical Systems, Inc. Due to 7F sheath introducers labeled as 7.5F
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 Merit Medical Systems, Inc. directly.
Affected Products
Custom Procedure Kit, REF: K12T-11077
Quantity: 24
Why Was This Recalled?
7F sheath introducers labeled as 7.5F
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Merit Medical Systems, Inc.
Merit Medical Systems, Inc. has 135 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report