Medical Device Recalls
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1 result found
510(K) Number: K090847 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Platelia Toxo IgM Catalog Number 26211 UDI Code: 03610520005552 The Platelia Toxo IgM assay is a... | 2 | 09/04/2025 |
FEI # 3002701146 Bio-Rad Laboratories, Inc. |
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