Reported Oct 29, 2025 · Ongoing
Artegraft¿ Collagen Vascular Graft; REF: AG1015;
LeMaitre Vascular, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: LeMaitre Vascular, Inc. · 206 N Center Dr · North Brunswick, NJ · 08902-4246
Is this the product you have?
- Artegraft¿ Collagen Vascular Graft
- REFAG1015
- Lot codes and dates
- REFAG1015
- UDI-DI00316837000343
- Lot/Serial Number23MM581-016
- Amount recalled
- 1 unit
Where it was sold
Why it was recalled
The device was incorrectly packed in the wrong size labeled outer packaging.
This product could cause temporary or reversible health problems — stop using it.
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