Philips Ultrasound, Inc: Medical Device Recall in 2025 - (Recall #: Z-2375-2025)

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:

L12-5 38mm Transducer Probe

Product Classification:

Class III

Date Initiated: July 3, 2025

Date Posted: September 3, 2025

Recall Number: Z-2375-2025

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. 989605428532; UDI: (01)00884838073623(21)B305XD, (01)00884838073623(21)F05R7X, (01)00884838073623(21)B1Y35V, (01)00884838073623(21)B305ZX, (01)00884838073623(21)F05K8W, (01)00884838073623(21)B3GWRJ, (01)00884838073623(21)B1Y306, (01)00884838073623(21)B1Y3CG, (01)00884838073623(21)B1Q699, (01)00884838073623(21)B1Y3C4, (01)00884838073623(21)B1RXWK, (01)00884838073623(21)B305X5, (01)00884838073623(21)B305ZK, (01)00884838073623(21)B3NFD5, (01)00884838073623(21)F034C6; Serial No. B305XD, F05R7X, B1Y35V, B305ZX, F05K8W, B3GWRJ, B1Y306, B1Y3CG, B1Q699, B1Y3C4, B1RXWK, B305X5, B305ZK, B3NFD5, F034C6.

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated