Medical Device Recalls
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191 to 191 of 191 Results
510(K) Number: K042489 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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SHERPA NX ACTIVE GUIDING CATHETER, 6F, SR4.0, 100CM, 070", REF SA6SR40. for cardiovascular use | 1 | 10/01/2019 | Medtronic Vascular |
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