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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
Recall Number: Z-1359-2014
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Dengue NS1 Ag/IgG/M Ab Duo Test Card; LumiQuick. Santa Clara, CA 95054 2 04/07/2014 FEI # 3005984081
LumiQuick Diagnostics Inc.
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