LeMaitre Vascular, Inc. is recalling one unit of the Artegraft Collagen Vascular Graft (REF: AG1015) because it was placed in the wrong size labeled outer packaging. This recall involves Lot/Serial Number 23MM581-016 and affects one unit distributed to Arkansas. A clinician may open the package expecting one size but receive another, which can cause delays or complications during surgical procedures. If you have this device in your inventory, you should contact the manufacturer immediately to arrange for a return or replacement.
The mismatch between the label on the outer packaging and the actual size of the device inside can lead to surgical delays if the surgeon discovers the error during a procedure. This mismatch creates a risk of using an incorrectly sized graft or needing to open additional sterile packaging during surgery.
Firm initiated recall via letter notification.
Quantity: 1 unit
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES · Raw API Response
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