Medical Device Recalls
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1 result found
Recall Number: Z-1013-2017 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| UniCel DxH 800 Coulter Cellular Analysis System, Catalog No. 629029, B24465, B24802, B68304 | 2 | 01/11/2017 |
FEI # 2050012 Beckman Coulter Inc. |
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