Medical Device Recalls
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1 result found
510(K) Number: K842115 |
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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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ULTRA Fabric Reinforced surgical Gown X-Large Sterile The product is a sterile, single use, surgi... | 2 | 11/07/2012 | Kimberly-Clark Corporation |
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