Medical Device Recalls
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1 result found
510(K) Number: K171792 |
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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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| Product Name: ID NOW" Influenza A & B 2 Model/Catalog Number: 427-000 Software Version: Not Applic... | 2 | 03/13/2026 |
FEI # 1221359 Abbott Diagnostics Scarborough, Inc. |
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