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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 19 Results
Related Medical Device Recalls
 
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Z-2218-2025 - Upgrade to MR 7700 Model Number (REF): 782130; 2 07/30/2025 Philips North America
Z-2216-2025 - SmartPath to dStream for XR and 3.0T Model Numbers (REF): (1) 781270, (2) 782113, (3) 782129; 2 07/30/2025 Philips North America
Z-2215-2025 - SmartPath to dStream for 3.0T Model Number (REF): 782145; 2 07/30/2025 Philips North America
Z-2217-2025 - SmartPath to Ingenia Elition X Model Numbers (REF): (1) 782118, (2) 782144; 2 07/30/2025 Philips North America
Z-2214-2025 - MR 7700 Model Numbers (REF): (1) 782120, (2) 782153; 2 07/30/2025 Philips North America
Z-2213-2025 - MR 5300 Model Numbers (REF): (1) 782110, (2) 782135 (China ONLY), (3) 782152; 2 07/30/2025 Philips North America
Z-2212-2025 - Intera 3.0T Quasar Dual Model Number (REF): 781150; 2 07/30/2025 Philips North America
Z-2211-2025 - Ingenia Elition X Model Numbers (REF): (1) 781358, (2) 782107, (3) 782119, (4) 782136, (5) 782151 (China ONLY); 2 07/30/2025 Philips North America
Z-2210-2025 - Ingenia Elition S Model Numbers (REF): (1) 781357, (2) 782106, (3) 782137, (4) 782150 (China ONLY); 2 07/30/2025 Philips North America
Z-2209-2025 - Ingenia Ambition X Model Numbers (REF): (1) 781356, (2) 782109, (3) 782138; 2 07/30/2025 Philips North America
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