Class IIIReported 2026-04-01

Philips X3-1 Ultrasound Transducer

Recalled by Philips Ultrasound, Inc

Reason for Recall

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

Recall Number

Z-1627-2026

Classification

Class III

Status

Ongoing

Category

device

Initiated

2025-09-05

Reported

2026-04-01

Distribution

US Nationwide distribution.

Code Info

Model No. 989605440742, 989603002321, 989605388101, 989605440741; UDI: (01)00884838067615(21)033TVZ, (01)00884838067615(21)02Q8R3, (01)00884838067615(21)02VLZV, (01)00884838067615(21)02WND0, (01)00884838067615(21)02ZWBH, (01)00884838067615(21)02GP3C, (01)00884838067615(21)03DTL6, (01)00884838067615(21)02JK1H, (01)00884838067615(21)02VMJ6, (01)00884838067615(21)035Z89, (01)00884838067615(21)031C21, (01)00884838067615(21)02JL3W, (01)00884838067615(21)03C066, (01)00884838067615(21)02JK8D; Serial No. 033TVZ, 02Q8R3, 02VLZV, 02WND0, 02ZWBH, 02GP3C, 02YHTG, 02YHPN, 03DTL6, 02JK1H, 02VMJ6, 035Z89, 031C21, 038NQC, 02JL3W, 03C066, 02JK8D.

Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.