Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K211594 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Stryker Neurovascular, Trevo Trak 21 Microcatheter, REF 90338, 0.021in X162cm | 2 | 02/14/2024 |
FEI # 3012931345 Stryker, Inc. |
| Trevo Trak 21 Microcatheter, Catalog: 90338 | 2 | 05/28/2024 |
FEI # 3008853977 Stryker Neurovascular |
| The Trevo Trak 21 Microcatheter is a single-lumen, braided shaft, variable stiffness catheter with r... | 2 | 10/07/2024 |
FEI # 3008853977 Stryker Neurovascular |
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