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 recall affects specific serial numbers and requires immediate attention from medical professionals using the product.
The grafts may develop small holes at the seam lines during surgical use, leading to bleeding at the graft connections. This can compromise the surgical procedure and patient safety if not addressed.
Medical professionals using the Hemashield Platinum Vascular Grafts for arterial repair or replacement are most at risk. The recall applies to specific serial numbers listed in the official notice.
Check the serial number on the product. Affected units have specific serial numbers listed in the recall notice, including 1071592227, 1076652332, and other numbers provided in the official list.
Verify the product's serial number against the list of affected numbers provided in the recall notice.
The grafts may have small holes at the seam lines, which can cause bleeding during surgical procedures.
Check the serial number against the list of affected numbers provided in the recall notice, which includes specific serial numbers like 1071592227 and 1076652332.
The recall does not specify a remedy, so contact the manufacturer directly for guidance.
We’ve drafted a message you can send Maquet to request your refund or repair — edit it as you like.
Subject: Recall Z-1874-2020 — Maquet Maquet Hello, I own a Maquet that is covered by recall Z-1874-2020 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.
