PHILIPS HEADQUARTERS CAMBRIDGE: Medical Device Recall in 2023 - (Recall #: Z-1623-2023)

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

Product Classification:

Class II

Date Initiated: April 12, 2023

Date Posted: May 31, 2023

Recall Number: Z-1623-2023

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: 22 units

Code Information:

UDI-DI: (01)00884838085015(21) Serial Numbers: 75592542 81629039 82435668 84375501 85146962 85469672 86188405 86188817 86820074 87367597 92174932 92622328 92637836 92680372 92823844 92870027 92889235 94581069 95050209 95055576 96094114 96462378 Serial Numbers: 75592542 81629039 82435668 84375501 85146962 85469672 86188405 86188817 86820074 87367597 92174932 92622328 92637836 92680372 92823844 92870027 92889235 94581069 95050209 95055576 96094114 96462378

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