Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Artegraft¿ Collagen Vascular Graft Recalled by LeMaitre Vascular, Inc. Due to The device was incorrectly packed in the wrong...
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 LeMaitre Vascular, Inc. directly.
Affected Products
Artegraft¿ Collagen Vascular Graft; REF: AG1015;
Quantity: 1 unit
Why Was This Recalled?
The device was incorrectly packed in the wrong size labeled outer packaging.
Where Was This Sold?
This product was distributed to 1 state: AR
About LeMaitre Vascular, Inc.
LeMaitre Vascular, Inc. has 69 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report