Philips Ultrasound, Inc: Medical Device Recall in 2025 - (Recall #: Z-2407-2025)

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:

X3-1 Transducer Probe

Product Classification:

Class III

Date Initiated: July 3, 2025

Date Posted: September 3, 2025

Recall Number: Z-2407-2025

Event ID: 97217

Reason for Recall:

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

Status: Ongoing

Product Quantity: 171,322 units

Code Information:

Model No. 989605388101, 21715A; UDI: N/A; Serial No. 02YHPN, 02JK1H.

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated