Reported Mar 25, 2026 · Ongoing
Artegraft Vascular Graft; REF#: AG740;
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 Vascular Graft; REF#: AG740;
- Lot codes and dates
- REF#: AG740
- UDI-DI00316837000299
- Serial Number24GG298-022
- Expiration Date28Jun2027
- Amount recalled
- 1 unit
Where it was sold
- Nationwide
- IL
Why it was recalled
Labeling mix-up resulting in the incorrect lot outer packaging of product.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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