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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-2993-2018
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Diagnostica Stago STA N®oplastine® CI Plus, 10 ml vial. In-Vitro Diagnostic for determination of t... 2 09/07/2018 FEI # 2245451
Diagnostica Stago, Inc.
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