Medical Device Recalls
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1 result found
Recall Number: Z-0321-2021 |
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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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| Ultra2 Resolution Variants System for Abnormal Hemoglobin Quantitation | 2 | 10/31/2020 |
FEI # 1931251 Primus Corporation |
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