LeMaitre Vascular recalls Artegraft Vascular Graft (REF# AG740) due to incorrect labeling causing potential confusion in product identification. This affects medical devices used in vascular procedures.
Labeling mix-up resulting in the incorrect lot outer packaging of product.
LeMaitre Vascular is recalling Artegraft Vascular Grafts with specific serial numbers and expiration dates due to a labeling mix-up. This could lead to confusion about which product is being used, potentially affecting medical procedures.
The recall is due to a labeling mix-up where the outer packaging of the product has the wrong lot information. This could cause confusion about which graft is being used, potentially leading to incorrect medical procedures.
Medical professionals and patients who use Artegraft Vascular Grafts with the specified serial numbers and expiration dates are likely affected. Those in surgical settings using these grafts are at the highest risk.
Check for the serial number 24GG298-022 and expiration date of June 28, 2027 on the packaging. The product is identified by the reference number AG740 and unique device identifier 00316837000299.
Verify the serial number and expiration date on the packaging to confirm if it matches the recalled items.
The recall is due to a labeling mix-up resulting in the incorrect lot outer packaging of the product.
The official notice does not specify a remedy, so check the product labeling to confirm if it matches the recalled items.
The recall is for labeling confusion, not a direct safety hazard, so the risk is low.
We’ve drafted a message you can send LeMaitre Vascular to request your refund or repair — edit it as you like.
Subject: Recall Z-1574-2026 — LeMaitre Vascular LeMaitre Vascular Hello, I own a LeMaitre Vascular that is covered by recall Z-1574-2026 from LeMaitre Vascular. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
