Philips Ultrasound, Inc: Medical Device Recall in 2025 - (Recall #: Z-2362-2025)

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:

C9-3v Transducer Probe

Product Classification:

Class III

Date Initiated: July 3, 2025

Date Posted: September 3, 2025

Recall Number: Z-2362-2025

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. 989605366341; UDI: (01)00884838024304(21)B0LBJX, (01)00884838024304(21)B0LBXV; Serial No. B0DCXF, B0CT9W, 038VLZ, B0LBY2, 037RDB, B0DD3B, B0LBJX, B0LBXV, 037RG6, B0JDHK, B0BMR8.

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated