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FDA (Device enforcement)Recalled 2025-05-13class ii

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

Hazard

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Details from the source

Reason for recall: Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application. Distribution: Worldwide distribution - US Nationwide and the countries of Andorra, Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, Colombia, C¿te D'Ivoire, Cyprus, Czech Republic, Denmark, Finland, France, French Guiana, Georgia, Germany, Greece, Guadeloupe, Hong Kong, Iceland, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Kenya, Latvia, Lebanon, Libya, Lithuania, Malaysia, Malta, Marti Quantity: 28 units (5 US, 23 OUS) 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;

UPC codes

00884838099739, 00884838108660

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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