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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-0618-2016
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Siemens Acute Care MYO DilPak Catalog Number: CMYO-D SMN:10445081 in vitro diagnostic 2 01/07/2016 FEI # 3002637618
Siemens Healthcare Diagnostics Inc
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