HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch, Product Code: M00202175824P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Serial Numbers: 1069833603 1069800979 1069830915 1069822813 1069826494 1073232852 1073244538 1073248356 1073247694 1073238111 1073244655 1073245805 1074078868 1074096981 1073245180 1075816095 1075833820 1075817616 1075822171 1121372880 1121440106 1121438219 1121372041 1121396486 1121390993 1121413834 1121410287 1123883969 1123881709 1123882605 1126691350 1131379994 1150412103 1150432593 1150316987 1150489896 1150511448 1150483701 1162227315 1162227920 1162231345 1177013851 1176957069 1177022361 1177037106 1177062054 1180553781 1180752802 1184425670 1073247948 1073255445 1075827022 1080534907 1120128533 1120067440 1121368128 1121428442 1121415860 1123880071 1150432730 1150485356 1150485473 1180546087 1184503258 1187865172
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Maquet Cardiovascular, LLC
- Reason for Recall:
- Potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch, Product Code: M00202175824P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Product Codes/Lot Numbers:
Serial Numbers: 1069833603 1069800979 1069830915 1069822813 1069826494 1073232852 1073244538 1073248356 1073247694 1073238111 1073244655 1073245805 1074078868 1074096981 1073245180 1075816095 1075833820 1075817616 1075822171 1121372880 1121440106 1121438219 1121372041 1121396486 1121390993 1121413834 1121410287 1123883969 1123881709 1123882605 1126691350 1131379994 1150412103 1150432593 1150316987 1150489896 1150511448 1150483701 1162227315 1162227920 1162231345 1177013851 1176957069 1177022361 1177037106 1177062054 1180553781 1180752802 1184425670 1073247948 1073255445 1075827022 1080534907 1120128533 1120067440 1121368128 1121428442 1121415860 1123880071 1150432730 1150485356 1150485473 1180546087 1184503258 1187865172
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1870-2020
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