Maquet recalls Hemashield Platinum Woven Double Velour Vascular Grafts with potential small holes at seam lines causing intra-operative bleeding. Affected units have specific serial numbers.
Potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts
Maquet is recalling Hemashield Platinum Vascular Grafts that may have small holes at seam lines, which could cause bleeding during surgery. This is a serious risk for patients undergoing vascular repair procedures.
The grafts may develop small holes at the seam lines during surgical use, leading to bleeding at the graft connections. This could cause significant blood loss during the procedure if the grafts are used in arterial repairs.
Medical professionals using the Hemashield Platinum Vascular Grafts for arterial repair procedures are most at risk. Patients who have received these grafts during surgery may also be affected.
Check if your Hemashield Platinum Vascular Graft has a serial number listed in the provided list (e.g., 1069844373, 1070838372). The product is used for arterial repair procedures in patients with aneurysms or occlusive disease.
Immediately stop using the recalled Hemashield Platinum Vascular Grafts if you have them.
The grafts may have small holes at the seam lines, which can cause bleeding during surgery.
Check if your graft's serial number is listed in the provided list of numbers (e.g., 1069844373, 1070838372).
Yes, if you have the recalled graft, contact your surgeon immediately to discuss the risk of bleeding during surgery.
We’ve drafted a message you can send Maquet to request your refund or repair — edit it as you like.
Subject: Recall Z-1873-2020 — Maquet Maquet Hello, I own a Maquet that is covered by recall Z-1873-2020 from Maquet. 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.
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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.