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Philips North America Llc recalls 728306 Brilliance iCT-Computed Tomography X-ray systems 728305 Brilliance iCT Upgrades
Recalled August 25, 2021 · FDA recall Z-2314-2021 · Philips North America
Hazard
When setting patient weight unit preferences to pounds, SynchRight P3T (Personalized Patient Protocol) software will result in increased contrast volume, resulting in increased contrast volume recommended for the patient. · FDA Class II
Units
3 units
Sold at
US Nationwide distribution in the states of AZ, FL, LA, MN, NE, NV, NY, PA.
Description
When setting patient weight unit preferences to pounds, SynchRight P3T (Personalized Patient Protocol) software will result in increased contrast volume, resulting in increased contrast volume recommended for the patient.
Product
728306 Brilliance iCT-Computed Tomography X-ray systems 728305 Brilliance iCT Upgrades
Manufacturer(s)
Philips North America Llc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →