Medical Device Recalls
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1 result found
510(K) Number: K110951 |
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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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| CONSTELLATION ULTRAVIT 10K and CONSTELLATION HYPERVIT 20K, Description/REF: 25+ TOTALPLUS CP PAK 20... | 2 | 11/21/2025 | Alcon Research LLC |
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