Medical Device Recalls
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1 result found
510(K) Number: K071442 |
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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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| Neptune Plus, HEMOSTASIS PAD WITH ANTIMICROBIAL BARRIER, For hemostasis following needle/sheath remo... | 2 | 11/18/2015 |
FEI # 1000127185 TZ Medical Inc. |
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