ImaCor recalls ClariTEE Miniaturized TEE probe model CLT-010 due to potential reversed articulation causing improper probe movement. Affected units sold with Mobile Ultrasound.
Production assembly error resulting in the potential for reversed articulation, where moving the lever forward caused the probe tip to anteflex rather than retroflex, and vice versa.
ImaCor is recalling its ClariTEE Miniaturized TEE probe model CLT-01: a small ultrasound probe that may move incorrectly during use. This could lead to improper placement or injury if the probe tip bends in the wrong direction.
The probe may move in the opposite direction when the lever is moved, causing the tip to bend incorrectly instead of moving as intended. This could lead to improper placement or injury if the probe tip bends in the wrong direction.
Medical professionals using the ClariTEE Miniaturized TEE probe with Mobile Ultrasound systems are most likely affected. Patients using the probe may be at risk if the probe moves incorrectly.
Check for model number CLT-010 on the probe. The probe was sold with Mobile Ultrasound systems and has a unique identifier starting with 00861589000108.
Look for model number CLT-010 on the probe.
The probe may move in the opposite direction when the lever is moved, causing the tip to bend incorrectly instead of moving as intended.
Check for model number CLT-010 on the probe. The probe was sold with Mobile Ultrasound systems and has a unique identifier starting with 00861589000108.
The recall does not specify a remedy, so contact ImaCor for further instructions.
We’ve drafted a message you can send ImaCor to request your refund or repair — edit it as you like.
Subject: Recall Z-0038-2026 — ImaCor ImaCor Hello, I own a ImaCor that is covered by recall Z-0038-2026 from ImaCor. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
