Medical Device Recalls
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1 result found
510(K) Number: K905224 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Sarns Malleable Venous Return Cannulae 24, 28, 30, 32, 34, 36 & 40 Fr single stage with 3/8" & 1/2 f... | 2 | 07/23/2014 |
FEI # 1828100 Terumo Cardiovascular Systems Corporation |
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