Philips North America Llc recalls Product Name: SmartPath to dStream for XR and 3.0T; Model N
Recalled Product
Product Name: SmartPath to dStream for XR and 3.0T; Model Numbers: (1) 781270, (2) 782113;
Hazard / Issue
Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Model Numbers: (1) 781270, (2) 782113; UDI-DI: (1) 00884838095083, (2) 00884838098909; Serial Numbers: (1) 17283, 17299, 17321, 17356, 17357, 17369, 17378, 17398, 17416, 17425, 17473, 17490, 17499, 17550, 17564, 17565, 17569, 17589, 17590, 17594, 23026, 24012, 24023, 24066, 24075, 24087, 24090, 24110, 34107, 34152, 35043, 35047, 35056, 38004, 38023, 38084, 38089, 38113, 38120, 38199, 38202, 38300, 38366, (2) 17252, 17258, 17346, 24039, 24077, 24146, 34131, 34212, 35071, 38197, 38234, 38291;
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