Medical Device Recalls
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1 result found
510(K) Number: K790314 |
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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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Medex MX821L 72 inch (182.9cm) Administration Sets, Standard Drip, Sterile Single Use, Latex Free de... | 3 | 07/30/2008 | Smiths Medical Asd Inc |
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