Philips North America Llc recalls Product Name: SmartPath to dStream for 3.0T; Model Number: 782145
- Recall date
- May 13, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1789-2025
- FDA classification
- Class II
- Brand / firm
- Philips North America Llc
- Sold / distributed
- 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, Ir…
Why it was recalled
Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Product Name: SmartPath to dStream for 3.0T; Model Number: 782145
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