medical Class II Updated 2025-05-28

Philips North America Llc recalls Product Name: Evolution Upgrade 3.0T; Model Numbers: (1) 78

Recalled Product

Product Name: Evolution Upgrade 3.0T; Model Numbers: (1) 782117, (2) 782143;


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) 782117, (2) 782143; UDI-DI: (1) 00884838099739, (2) 00884838108660; Serial Numbers: (1) 42023, 42024, 42078, 42375, 42402, 42408, 71348, 85675, 85687, 85694, 85705, (2) 42193, 42225, 42308, 42320, 42366, 42415, 71595, 71815, 71836, 85649, 85684, 85688, 85690, 85695, 85697, 85699, 85708;
View official government recall

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