Medical Device Recalls
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1 result found
510(K) Number: K865056 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Natrelle CUI Series Tissue Expanders. Product Usage: Natrelle CUI Series Tissue Expander has bee... | 2 | 07/18/2015 | Allergan Inc |
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