Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K000313 |
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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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| 1) Vascular Dilator, Sterile EO, Rx Only, Catalog #: DIL-100-12; 2) Dilator, Sterile EO, Rx Only... | 2 | 07/27/2018 |
FEI # 3000718472 Galt Medical Corporation |
| Microintroducer Kit, 5F, Tearaway Sheath/Dilator PG, Catalog Number 45-901 | 2 | 06/14/2018 |
FEI # 3017892510 Angiodynamics Inc. (Navilyst Medical Inc.) |
| Tearaway Introducers, Catalog #: a) BNS-000-07, b) BNS-000-10; c) DIL-015-50; d) DSS-005-11; e... | 2 | 07/27/2018 |
FEI # 3000718472 Galt Medical Corporation |
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