Philips Ultrasound, Inc: Medical Device Recall in 2025 - (Recall #: Z-2361-2025)

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:

C9-3io Transducer Probe

Product Classification:

Class III

Date Initiated: July 3, 2025

Date Posted: September 3, 2025

Recall Number: Z-2361-2025

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. 989605395612; UDI: (01)00884838061538(21)B2CYBN, (01)00884838061538(21)B0WM4Z, (01)00884838061538(21)B0WM4P; Serial No. B2CYBN, B0WM4Z, B0WM4P.

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated