Medical Device Recalls
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1 result found
Recall Number: Z-1211-2026 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Ingenia Elition S. Product Code (REF): (1) 781357, (2) 782106, (3)782137. MR systems with SW ver... | 2 | 01/29/2026 |
FEI # 3006648320 Philips North America |
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