Medical Device Recalls
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1 result found
510(K) Number: K920974 |
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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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| remel BactiDrop Acridine Orange, REF 21502, 50 per package. | 2 | 10/30/2024 | Remel, Inc |
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