Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K063015 |
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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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DrugCheck, Manufactured by: Express Diagnostics Int;l Inc. 1550 Industrial Drive, Blue Earth MN 5601... | 2 | 05/27/2011 | Express Diagnostics Int'l., Inc. |
Drug Check, Distributed by Express Diagnostics Intl Inc., 1550 Industrial Drive, Blue Earth, MN 56... | 2 | 08/31/2011 | Express Diagnostics Int'l., Inc. |
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