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Philips North America Llc recalls Product Name: Upgrade to MR 7700; Model Number: 782130;
Recalled May 28, 2025 · FDA recall Z-1792-2025 · Philips North America
Hazard
Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application. · FDA Class II
Units
13 units (7 US, 6 OUS)
Sold at
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, Martinique, Mexico, Moldova, Monaco, Netherlands, New Zealand, Norway, Palestine, Philippines, Poland, Portugal, Qatar, Romania, Russian Fed., Serbia, Slovenia, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, Ukraine, United Kingdom, U.A.E.
Description
Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
Product
Product Name: Upgrade to MR 7700; Model Number: 782130;
Manufacturer(s)
Philips North America Llc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →