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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-1967-2026
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Philips SmartPath to dStream for XR and 3.0T with MR Elastography (MRE). 1. Model Number (REF): ... 2 04/27/2026 FEI # 3006648320
Philips North America
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