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Philips Ultrasound, Inc recalls SCNHD LA L7-4 HDI Transducer Probe
Recalled September 3, 2025 · FDA recall Z-2400-2025 · Philips Ultrasound
Hazard
To provide clarification and labelling to define the useful life of ultrasound transducers in the field. · FDA Class III
Units
171,322 units
Sold at
US Nationwide distribution.
Description
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Product
SCNHD LA L7-4 HDI Transducer Probe
Manufacturer(s)
Philips Ultrasound, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →