Medical Device Recalls
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1 result found
510(K) Number: K232567 |
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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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| NICO Myriad Illumination Pack Product No. NN-1000 11g Illumination Sleeve/Fiber; Product No. NN... | 2 | 11/26/2025 | Stryker Corporation |
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