WhichRecall
Class IIIReported 2026-04-01

Philips X7-2 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.

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Recall Number
Z-1628-2026
Classification
Class III
Status
Ongoing
Category
device
Initiated
2025-09-05
Reported
2026-04-01
Distribution
US Nationwide distribution.
Code Info
Model No. 989605388121, 989605347571, 989605347573; UDI: (01)00884838061729(21)0344RZ; Serial No. 03FG1T, 031LM2, 032Q7G, 0344RZ, 033VM9.
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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