Philips Ultrasound, Inc recalls L12-5 38mm Transducer Probe
- Recall date
- July 3, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2375-2025
- FDA classification
- Class III
- Brand / firm
- Philips Ultrasound, Inc
- Sold / distributed
- US Nationwide distribution.
Why it was recalled
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
L12-5 38mm Transducer Probe
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