Medical Device Recalls
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1 result found
510(K) Number: K952074 |
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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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| CLEARLINK System Non_DEHP Extenstion Set, Straight-Type Extension Set, Standard Bore, 1.2 Micron Fi... | 2 | 10/16/2025 |
FEI # 1417572 Baxter Healthcare Corporation |
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