Philips North America Llc: Medical Device Recall in 2024 - (Recall #: Z-1756-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

The Oncology Essentials Package of the Spectral CT imaging system.

Product Classification:

Class II

Date Initiated: March 29, 2024

Date Posted: May 8, 2024

Recall Number: Z-1756-2024

Event ID: 94352

Reason for Recall:

Potential for third party oncology marking laser to be reflected off the gantry cover surface, which can potentially lead to misdiagnosis and subsequent incorrect treatment.

Status: Ongoing

Product Quantity: 12 units

Code Information:

Model No. 728333; UDI: (01)00884838101111(21); Serial No. 10069, 10084, 10169, 10137, 10163, 10196, 10181, 10199, 10210, 10206, 10202, 10139.

Distribution Pattern:

Worldwide distribution - US Nationwide in the states of AZ, HI, MN, VT, WV and the countries of China, Macao, New Zealand, Portugal, Switzerland.

Voluntary or Mandated:

Voluntary: Firm initiated