Class III
Medical Device Recall: X8-2t Transducer Probe
Philips Ultrasound, Inc · July 3, 2025
Reason for Recall
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Distribution
US Nationwide distribution.
States Affected
NATIONWIDE
Quantity Affected
171,322 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2413-2025
Status: ongoing
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