Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K954848 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Hemashield Gold Woven and Knitted Double Vascular Grafts. | 2 | 07/22/2010 |
FEI # 2242352 Maquet Cardiovascular, LLC |
| Hemashield Gold Knitted Microvel Double Velour Vascular Graft-Axillo-bifemoral, Product Code: M00202... | 2 | 05/04/2020 |
FEI # 2242352 Maquet Cardiovascular, LLC |
| Hemashield Gold Knitted Microvel Double Velour Vascular Graft-Axillo-bifemoral, Product Code: M00202... | 2 | 05/04/2020 |
FEI # 2242352 Maquet Cardiovascular, LLC |
| Hemashield Gold Knitted Microvel Double Velour Vascular Graft Axillo-bifemoral, Product Code: M00202... | 2 | 05/04/2020 |
FEI # 2242352 Maquet Cardiovascular, LLC |
| Hemashield Gold Knitted Bifurcated, 18 mm x 9 mm; reference number M002020851890 | 2 | 12/20/2021 |
FEI # 2242352 Maquet Cardiovascular, LLC |
| HEMASHIELD GOLD KNITTED MICROVEL DOUBLE VELOUR VASCULAR GRAFT- D: 7 mm; L: 60 cm Indicated for use... | 2 | 03/07/2022 |
FEI # 2242352 Maquet Cardiovascular, LLC |
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