Medical Device Recalls
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1 result found
510(K) Number: K180545 |
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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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| VACUETTE SAFELINK, REF: 450210 | 2 | 01/03/2025 |
FEI # 3000974732 Greiner Bio-One GmbH |
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