Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Z-1349-2023 - Abbott Alinity m System, REF 08N53-002, containing Amplification Detetction Unit (ADU) #4. | 2 | 04/06/2023 |
FEI # 3005248192 Abbott Molecular, Inc. |
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