medical Class II Updated 2018-04-25

Philips Electronics North America Corporation recalls Conversion SmarthPath to dStream for 1.5T, Model 781260 P

Recalled Product

Conversion SmarthPath to dStream for 1.5T, Model 781260 Product Usage: Indicated for use as a diagnostic device. It can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body,or extremities.


Hazard / Issue

Potential risk for helium gas inside the MR examination room during a magnet quench

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: (Added 6/25/18): 39005 20071 18673 8715 8971 8165 8996 39024 10077 18528 32174 8578 10058 21290 10703
View official government recall

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