Philips North America: Medical Device Recall in 2023 - (Recall #: Z-1586-2023)

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:

Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72813

Product Classification:

Class II

Date Initiated: March 20, 2023

Date Posted: May 24, 2023

Recall Number: Z-1586-2023

Event ID: 92117

Reason for Recall:

Multi-Function Foot Switch Unload Pedal Foot Entrapment-Pressing the Unload Pedal of the foot switch to perform the unload function may cause entrapment of the operator's foot and injury

Status: Ongoing

Product Quantity: 3 units US ;2 units OUS

Code Information:

UDI-DI:(01)00884838085015(21) + Serial number US Serial Numbers: 33041, 500301, 500252. OUS Serial Numbers: 33040, 500408

Distribution Pattern:

Worldwide - US Nationwide distribution in the states of AR, CA, FL, IL, IN, MI, MO, NY, TN, TX, VT and the countries of Australia, Chile, Costa Rica, Czech Republic, Dominican, Republic Germany, India, Israel, Japan, Lithuania, Philippines, Poland, Sint Maarten (Dutch part), South Africa, Thailand, United Kingdom, Utd. Arab. Emir.

Voluntary or Mandated:

Voluntary: Firm initiated