Medical Device Recalls
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1 result found
Recall Number: Z-1136-2014 |
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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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| PRE1001US: Prevena Peel and Place System Kit (US-ONLY) Product Usage: The Prevena Incision Mana... | 2 | 03/05/2014 |
FEI # 3009897021 KCI USA, INC. |
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