Medical Device Recalls
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1 result found
Recall Number: Z-0484-2026 |
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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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| BD Kiestra" Isolate Suspension Cuvette Array; Catalog No.: 246100; | 2 | 11/07/2025 |
FEI # 1119779 Becton Dickinson & Co. |
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