Medical Device Recalls
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1 result found
Recall Number: Z-2207-2025 |
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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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| Ingenia 3.0T CX Model Numbers (REF): (1) 781271, (2) 782105; | 2 | 07/30/2025 |
FEI # 3006648320 Philips North America |
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