Medical Device Recalls
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1 result found
Recall Number: Z-1212-2026 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Ingenia Elition X. Product Code (REF): (1) 781358, (2) 782107, (3) 782136. MR systems with SW ve... | 2 | 01/29/2026 |
FEI # 3006648320 Philips North America |
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