Medical Device Recalls
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1 result found
510(K) Number: K121641 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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MiniArc Pro Single incision Sling System, Model number / Product Reference 9000261, Lot 936405xxx. ... | 2 | 11/16/2015 | Astora |
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