Medical Device Recalls
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1 result found
510(K) Number: K042400 |
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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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Product is Mucotrol Concentrated Oral Gel Wafer contained in HDPE Bottle. | 2 | 02/07/2007 | Belcher Pharmaceuticals Inc. |
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