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Philips North America recalls MR 7700 Magnetic Resonance (MR) system, Product Numbers 782120 and 782130 (Upgrade to MR 7700)
Recalled August 16, 2023 · FDA recall Z-2397-2023 · Philips North America
Hazard
The system operator is able to bypass the SmokeDetector Interlock system locking mechanism after a smoke detection by power cycling the system. · FDA Class II
Units
640 total
Sold at
US Nationwide. Global Distribution.
Description
The system operator is able to bypass the SmokeDetector Interlock system locking mechanism after a smoke detection by power cycling the system.
Product
MR 7700 Magnetic Resonance (MR) system, Product Numbers 782120 and 782130 (Upgrade to MR 7700)
Manufacturer(s)
Philips North America
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →