Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K152090 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Reprocessed Agilis Steerable Introducer: indicated for introducing various cardiovascular catheters... | 2 | 10/09/2018 |
FEI # 3011276773 Sterilmed, Inc. |
| St. Jude Medical. Agilis NxT Steerable Introducer: B1-Directional, Medium Curl 22.4 mm, 71 cm, 6.5 F... | 1 | 12/29/2017 |
FEI # 3011276773 Sterilmed Inc |
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