Medical Device Recalls
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1 result found
510(K) Number: K031614 |
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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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Pump in Style Advanced (PNSA)Breast Pump; a daily use, double pump, electric powered breast pump; Ma... | 3 | 02/11/2011 | Medela Inc |
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