Health & Personal Care
HIGH
FDA DEVICE
ImaCor Recalls Miniaturized TEE Probe Due to Assembly Error
ImaCor recalled 45 units of the ClariTEE Miniaturized TEE probe on August 29, 2025, due to a production assembly error. The defect may cause the probe to articulate incorrectly, posing a risk to patient safety. Healthcare providers and patients must stop using the device immediately.
ImaCor
Production assembly