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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
Recall Number: Z-1215-2026
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SmartPath to dStream for 3.0T. Product Code (REF): 782145. MR systems with SW version R11.1 and ... 2 01/29/2026 FEI # 3006648320
Philips North America
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