HIGHFDA DEVICE
ESAOTE Endocavity Ultrasonic Probe E 3-12 Recall Affects 5 Units (2025)
ESAOTE recalled 5 Endocavity Ultrasonic Probe E 3-12 units sold in the United States to healthcare providers in NC and TX. A potential weakness in the probe body could cause liquid to leak from the terminal part of the casing near the cable. Healthcare providers and patients should stop using the device immediately and follow manufacturer instructions.
ESAOTE
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