Maquet Cardiovascular, LLC Recall: HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-
Maquet Cardiovascular, LLC Recall: HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Maquet Cardiovascular, LLC; Product: HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-1 Branch, Product Code: M00202175826P0 - Product Usage:
| Recalling firm | Maquet Cardiovascular, LLC |
|---|---|
| Product | HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-1 Branch, Product Code: M00202175826P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease. |
| 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 II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Worldwide distribution - US Nationwide distribution and the countries of Dubai, Argentina, Austria, Belgium, Brazil, Japan, Canada, China, Germany, Spain, Finland, France, UK, Hongkong, Italy, Korea, Netherlands, Poland, Serbia, Sweden. |
| Recall initiated | 20200407 |
| Recall number | Z-1871-2020 |
| Category | device |
| State | NJ |
| Country | United States |
$29/mo
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