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Philips North America Llc recalls 728332 IQon Spectral CT-Computed Tomography X-ray system
Recalled August 25, 2021 · FDA recall Z-2317-2021 · 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
N/A
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
728332 IQon Spectral CT-Computed Tomography X-ray system
Manufacturer(s)
Philips North America Llc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →