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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 13 Results
Related Medical Device Recalls
 
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Z-1214-2026 - Upgrade to MR 7700. Product Code (REF): 782130. MR systems with SW version R11.1 and R12.1. 2 01/29/2026 Philips North America
Z-1216-2026 - SmartPath to dStream for XR and 3.0T. Product Code (REF): 781270. MR systems with SW version R11.1 and R12.1. 2 01/29/2026 Philips North America
Z-1215-2026 - SmartPath to dStream for 3.0T. Product Code (REF): 782145. MR systems with SW version R11.1 and R12.1. 2 01/29/2026 Philips North America
Z-1213-2026 - MR 7700. Product Code (REF): (1) 782120, (2) 782153. MR systems with SW version R11.1 and R12.1. 2 01/29/2026 Philips North America
Z-1212-2026 - Ingenia Elition X. Product Code (REF): (1) 781358, (2) 782107, (3) 782136. MR systems with SW version R11.1 and R12.1. 2 01/29/2026 Philips North America
Z-1211-2026 - Ingenia Elition S. Product Code (REF): (1) 781357, (2) 782106, (3)782137. MR systems with SW version R11.1 and R12.1. 2 01/29/2026 Philips North America
Z-1210-2026 - Ingenia Ambition X. Product Code (REF): (1) 781356, (2) 782109, (3)782138. MR systems with SW version R11.1 and R12.1. 2 01/29/2026 Philips North America
Z-1209-2026 - Ingenia Ambition S. Product Code (REF): 782108. MR systems with SW version R11.1 and R12.1. 2 01/29/2026 Philips North America
Z-1207-2026 - Ingenia 3.0T. Product Code (REF): (1) 781342, (2) 781377. MR systems with SW version R11.1 and R12.1. 2 01/29/2026 Philips North America
Z-1208-2026 - Ingenia 3.0T CX. Product Code (REF): 781271. MR systems with SW version R11.1 and R12.1. 2 01/29/2026 Philips North America
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