Medical Device Recalls
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1 result found
510(K) Number: K081210 |
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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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Exel Safety Huber Infusion Sets (20G and 22G sizes with Catalog Numbers 37854S, 37855S. 37858S). | 1 | 01/22/2010 | Exelint International Co. |
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