Medical Device Recalls
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1 result found
510(K) Number: K193517 |
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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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| ViziShot 2FLEX. Single Use Aspiration Needle. Model Number: NA-U403SX-4019. The ViziShot 2 FLEX t... | 1 | 09/05/2025 | Olympus Corporation of the Americas |
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