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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 3 of 3 Results
510(K) Number: K050186
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FDA Recall
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SCREENERS Dip Drug Test, Catalog Number: SCD-7MB300 The SCREENERS Dip Drug Test is a one-step imm... 2 06/27/2011 Ameditech Inc
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.