Medical Device Recalls
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1 result found
Recall Number: Z-1201-2025 |
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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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| remel BLOOD AGAR EMB AGAR BIPLATE, REF R02041, QTY 100, for invitro diagnostic use | 2 | 02/20/2025 |
FEI # 1924669 Remel, Inc |
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