LeMaitre Vascular, Inc. recalls Artegraft¿ Collagen Vascular Graft; REF: AG1015;
- Recall date
- September 25, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0289-2026
- FDA classification
- Class II
- Brand / firm
- LeMaitre Vascular, Inc.
- Sold / distributed
- US distribution to the state of: AR
Why it was recalled
The device was incorrectly packed in the wrong size labeled outer packaging.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Artegraft¿ Collagen Vascular Graft; REF: AG1015;
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