Medical Device Recalls
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1 result found
510(K) Number: K212216 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Prismaflex ST Set: ST60 (product code 107643), ST100 (product code 107636), ST150 (product code 107... | 2 | 10/12/2022 | Baxter Healthcare Corporation |
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