ClearanceBrief
Recall Z-1623-2023 ยท JAK System, X-Ray, Tomography, Computed

PHILIPS HEADQUARTERS CAMBRIDGE

Incisive CT- Whole-body computed tomography (CT) X-Ray System Model Number: 728143 (OUS)

DateMay 23, 2023 (initiated Apr 12, 2023)
StatusOpen, Classified
ReasonPotential for Incorrect Image Orientation resulting images may be flipped or reversed result in misdiagnosis, incorrect treatment of a condition, or additional radiation exposure if a rescan is required
Root causeSoftware design
ActionPhilips issued Urgent Medical Device Correction Letters on 4/12/23 US consignees via Certified United States Postal Service (USPS) with delivery confirmation. International global markets were notified of the issue and instructed to distribute the FSN to affected consignees in accordance with local requirements. Letter states reason for recall, health risk and action to take: Refer to the IFU of your Incisive CT system to ensure proper use of the Precise Position function (IFU Section 4.9). " If the patient orientation automatically selected by Precise Position (see Figure 2) is inconsiste
Quantity22 units
DistributionAR, CA, OK, TX Foreign: Country Argentina Australia Austria China Colombia Czech Republic Dominican Rep France Germany Guadeloupe Hong Kong India Japan Kuwait Latvia Lithuania Netherlands Norway Portugal Romania Spain Switzerland Taiwan Thailand United Kingdom Vietnam
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K180015Philips Incisive CT
Philips Healthcare (Suzhou) Co., Ltd., Mar 20, 2018
K212441Philips Incisive CT
Philips Healthcare (Suzhou) Co., Ltd., Apr 27, 2022