Philips Healthcare (Suzhou) Co., Ltd.: Medical Device Recall in 2026 - (Recall #: Z-1003-2026)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2026.

Data Source: FDA.

Product Description:

Philips Incisive CT

Product Classification:

Class II

Date Initiated: December 3, 2025

Date Posted: January 14, 2026

Recall Number: Z-1003-2026

Event ID: 98238

Reason for Recall:

Potential for incomplete scan due to unstable connection inside of floating sensor.

Status: Ongoing

Product Quantity: 35

Code Information:

Distribution Pattern:

U.S. and U.S. territories

Voluntary or Mandated:

FDA Mandated