Medical Device Recalls
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41 to 41 of 41 Results
510(K) Number: K934127 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Terumo Sarns brand Soft-Flow Aortic Cannula with flange, angled, wire-reinforced, with Luer, 6 mm (1... | 2 | 11/23/2005 |
FEI # 1828100 Terumo Cardiovascular Systems Corp |
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