medical Class II Updated 2025-05-28

Philips North America Llc recalls Product Name: SmartPath to Ingenia Elition X; Model Numbers

Recalled Product

Product Name: SmartPath to Ingenia Elition X; Model Numbers: (1) 782118, (2) 782144;


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) 782118, (2) 782144; UDI-DI: (1) 00884838099746, (2) 00884838108677; Serial Numbers: (1) 42072, 42194, 42306, 71019, 71025, 71050, 85661, 85676, (2) 42062, 42105, 42323, 42346, 42441, 71278, 71504, 71508;
View official government recall

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