---
title: "ClariTEE Probe- Miniature transesophageal echo ultrasound probe for use with ... — FDA record Z-0231-2025 | Is It on Recall"
description: "Epoxy used to seal the edge of the transducer into its paddle exceeded specification. This variability could attenuate the ultrasound signal with a potential im"
url: https://isitonrecall.com/recall/fda-device-z-0231-2025-claritee-probe-miniature-transesophageal-echo-ultrasound-probe-for-use-with-imacor-ultrasound-diagno/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# ClariTEE Probe- Miniature transesophageal echo ultrasound probe for use with ImaCor ultrasound diagnostic platforms. ... — FDA record Z-0231-2025

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Sep 16, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: ClariTEE Probe- Miniature transesophageal echo ultrasound probe for use with ImaCor ultrasound diagnostic platforms. Model/Catalog Number: CLT-010, CLT-010-1
- **Reason**: Epoxy used to seal the edge of the transducer into its paddle exceeded specification. This variability could attenuate the ultrasound signal with a potential impact on the quality of images obtained from the probes.
- **Classification**: Class II
- **Recalling firm**: ImaCor Inc.
- **Quantity**: 73 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0231-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0231-2025%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI - Primary - 00861589000108 Lot numbers: 20250509 and 20250823 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

FL ,GA, NJ, TN

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Florida](https://isitonrecall.com/state/florida/)
- [Georgia](https://isitonrecall.com/state/georgia/)
- [New Jersey](https://isitonrecall.com/state/new-jersey/)
- [Tennessee](https://isitonrecall.com/state/tennessee/)

## Dates in the source

- **Report date**: Nov 6, 2024
- **Recall initiation date**: Sep 16, 2024
- **Center classification date**: Oct 25, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0231-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [ImaCor Inc. records](https://isitonrecall.com/brand/imacor-inc/)