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Recall Observatory FDA recall evidence

Device product

728306 Brilliance iCT-Computed Tomography X-ray systems 728305 Brilliance iCT Upgrades

Z-2314-2021

June 08, 2021

Class II

Product summary

Firm
Philips North America Llc
Event
Event 88336
Status
Terminated
Classification
Class II
Quantity
3 units
Official record key
device-enforcement:Z-2314-2021

Official wording

Reason: 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.

Code information: S/N UDI: 87013 (01)00884838059474(21)87013 87008 (01)00884838059474(21)87008 87011 (01)00884838059474(21)87011 Software Version 4.1.10 SynchRight Option

Distribution pattern: US Nationwide distribution in the states of AZ, FL, LA, MN, NE, NV, NY, PA.

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    software will result in