Medical Device Recalls
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1 result found
Recall Number: Z-1317-2026 |
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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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| Spectral CT; Product Code (REF): 728333; | 2 | 02/06/2026 |
FEI # 3016618143 Philips North America Llc |
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