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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-2216-2025
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SmartPath to dStream for XR and 3.0T Model Numbers (REF): (1) 781270, (2) 782113, (3) 782129; 2 07/30/2025 FEI # 3006648320
Philips North America
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