Medical Device Recalls
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1 result found
510(K) Number: K140225 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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EliA GBM Wells, Material Number 14551401, for Phadia 250, 2500, and 5000. In vitro diagnostic | 2 | 01/24/2024 | Phadia Ab |
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