Medical Device Recalls
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1 result found
510(K) Number: K030888 |
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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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Container fill and transfer sets, 250 mL, 500 mL, 1000 mL, 2000 mL, 3000 mL, or 4000 mL. | 2 | 07/22/2016 | The Metrix Company |
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