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-1190-2019 - BIOPHEN LMWH Control C4, REF 224201 | 3 | 04/17/2019 |
FEI # 3005017664 Aniara Diagnostica LLC |
| Z-1189-2019 - BIOPHEN UFH Control C1, REF 224101 | 3 | 04/17/2019 |
FEI # 3005017664 Aniara Diagnostica LLC |
| Z-1188-2019 - BIOPHEN UFH Control C2, REF 223901 | 3 | 04/17/2019 |
FEI # 3005017664 Aniara Diagnostica LLC |
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