PHILIPS HEADQUARTERS CAMBRIDGE: Medical Device Recall in 2023 - (Recall #: Z-1625-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

Incisive CT Plus -Whole-body computed tomography (CT) X-Ray System Model Number: 728149 (OUS)

Product Classification:

Class II

Date Initiated: April 12, 2023

Date Posted: May 31, 2023

Recall Number: Z-1625-2023

Event ID: 92238

Reason for Recall:

Potential 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

Status: Ongoing

Product Quantity: 5 units

Code Information:

UDI-DI: (01)00884838103474(21) Serial Number: 530537 554032 554060 554065 554078

Distribution Pattern:

AR, 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

Voluntary or Mandated:

Voluntary: Firm initiated