Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K103668 |
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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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| SharkCore LG Fine Needle Biopsy System (19GA); Material/Part#: DSL-19-01 | 2 | 02/28/2017 | Medtronic |
| SharkCore Fine Needle Biopsy System (25GA); Material/Part#: DSC-25-01 | 2 | 02/28/2017 | Medtronic |
| SharkCore Fine Needle Biopsy System (22 GA); Material/Part #s: DSC-22-01 | 2 | 02/28/2017 | Medtronic |
| BNX Fine Need Aspiration System (22GA); Material/Part#: DSN-22-01 | 2 | 02/28/2017 | Medtronic |
| BNX Fine Need Aspiration System (19GA); Material/Part #: DSN-19-01 | 2 | 02/28/2017 | Medtronic |
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