FDA Device recall Z-1872-2020
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch, Product Code: M00202175828P0 - Product Usage: for use in the replacement…
- FDA Device
- Class II
- terminated
- Published 2020-05-13
On 2020-05-13 the FDA classified a Class II recall of HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch, Product Code: M00202175828P0 - Product Usage: for use in the replacement… by Maquet Cardiovascular, citing potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1872-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-04-07 |
| Published | 2020-05-13 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Maquet Cardiovascular |
| Distribution | US |
Product
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch, Product Code: M00202175828P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Reason
Potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts
Identifiers
| code_info | Serial Numbers: 1069016915 1069016778 1069024392 1069023633 1069020945 1069017069 1069887359 1070175211 1070689212 10…Serial Numbers: 1069016915 1069016778 1069024392 1069023633 1069020945 1069017069 1069887359 1070175211 1070689212 1070691938 1070692229 1073307657 1073274083 1074239734 1074508943 1076726963 1076724195 1076691012 1080515527 1080502574 1080516052 1080521115 1080517807 1080517202 1080511104 1082496280 1107410936 1107401196 1107412006 1108349382 1108384849 1109527236 1109536351 1109582959 1109545837 1109638521 1109712993 1112019301 1112016613 1112016964 1112016730 1112017860 1112017489 1112018385 1112051221 1112030283 1113457118 1113461382 1113412574 1113446562 1113429579 1115826461 1115864128 1115914431 1115914548 1115827123 1115899734 1115897708 1115825331 1115890109 1115890226 1116687063 1116670058 1116665366 1116796185 1118783633 1118872362 1118683489 1118680938 1118706076 1118855516 1118677296 1118857425 1118863618 1118853607 1118865156 1118868449 1120124949 1120151826 1120162616 1120197246 1120115580 1121427175 1121369492 1121368479 1121432004 1121402790 112136772 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1872-2020%22
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