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U.S. Department of Health and Human Services

Medical Device Recalls
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Related Medical Device Recalls
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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Z-1188-2019 - BIOPHEN UFH Control C2, REF 223901 3 04/17/2019 Aniara Diagnostica LLC
Z-1190-2019 - BIOPHEN LMWH Control C4, REF 224201 3 04/17/2019 Aniara Diagnostica LLC
Z-1189-2019 - BIOPHEN UFH Control C1, REF 224101 3 04/17/2019 Aniara Diagnostica LLC
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