Medical Device Recalls
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1 result found
Recall Number: Z-3314-2026 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| SmartPath to dStream for 1.5T, SmartPath to dStream for 3.0T, SmartPath to dStream for XR and 3.0T,... | 2 | 09/25/2026 |
FEI # 3006648320 Philips North America |
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