Medical Device Recalls
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41 to 41 of 41 Results
510(K) Number: K934127 |
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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| 18 Fr 6mm Sft Flow Ang Wire W/L The Sarns Aortic Cannula is indicated for use in perfusion of the... | 2 | 12/03/2012 |
FEI # 1828100 Terumo Cardiovascular Systems Corporation |
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