Medical Device Recalls
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1 result found
510(K) Number: K991301 |
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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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CADD® High Volume Administration Set, REF 21-7081V-01, Sterile EO, Rx only, Made in Mexico, Smith M... | 2 | 01/17/2012 | Smiths Medical ASD, Inc. |
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