Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K161287 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Medtronic DxTerity(TM) TRA 5F, Diagnostic Catheter, REF U5TRAN35 | 3 | 09/26/2018 |
FEI # 1220452 Medtronic Vascular |
| Medtronic DxTerity Diagnostic Catheter, JL 4.0, REF DXT5JL40, marked with 6F color code on box. | 2 | 04/20/2018 |
FEI # 1220452 Medtronic Vascular |
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