Class III

Medical Device Recall: X11-4t Transducer Probe

Philips Ultrasound, Inc · July 3, 2025

Reason for Recall

To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

Distribution

US Nationwide distribution.

States Affected

NATIONWIDE

Quantity Affected

171,322 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2406-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Philips Ultrasound, Inc Medical Device Recall: X11-4t Transducer Probe | SafeCheck