Philips North America Llc: Medical Device Recall in 2025 - (Recall #: Z-1580-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

Zenition 50. Product Code 718096. The devices are used for radiological guidance and visualization during diagnostic, interventional and surgical procedures on all patients, except neonates (birth to one month), within the limits of the devices.

Product Classification:

Class II

Date Initiated: February 25, 2025

Date Posted: April 30, 2025

Recall Number: Z-1580-2025

Event ID: 96593

Reason for Recall:

A wireless foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation.

Status: Ongoing

Product Quantity: N/A

Code Information:

Product UDI: (01)00884838091535(21). 459801442981, Wireless foot switch set 3P (WFSS 3P) 459801238231, Wireless foot switch 3P, 459801257861, WFS Base Station 459800627394, Wireless foot switch set 3P 459800415535, Wireless foot switch 3P, 459800415542, WFS Base Station

Distribution Pattern:

Voluntary or Mandated:

FDA Mandated