Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K122459 |
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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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Posterior LITE w/ Capio SLIM; Model #M0068318150. Indicated for tissue reinforcement in women wit... | 2 | 05/04/2018 | Boston Scientific Corporation |
Uphold LITE w/ Capio SLIM; Model #M0068318170. Indicated for tissue reinforcement in women with p... | 2 | 05/04/2018 | Boston Scientific Corporation |
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