Medical Device Recalls
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1 result found
510(K) Number: K152876 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| AXS Infinity LS Long Sheath:((6F/.088in)/ x 70cm GEN-10800-70, (6F/.088in)/ x 80cm GEN-10800-80, (6F... | 2 | 09/28/2018 |
FEI # 3008853977 Stryker Neurovascular |
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