ClariTEE Probe- Miniature transesophageal echo ultrasound probe for use with ImaCor ultrasound diagnostic platforms. Model/Catalog Number: CLT-010, CLT-010-1
FDA Recall Z-0231-2025 · Posted 2024-10-25
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Recalling FirmImaCor Inc.
Recall StatusOpen, Classified
Product CodeITX
Date Initiated2024-09-16
Product Quantity73 units
Reason for Recall
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.
Firm Action
ImaCor issued Inventory Correction for ImaCor ClariTEE Probe (CLT-010 and CLT-010-1) letter on 9/16/24. Letter states reason for recall, health risk and action to take:
1. Identify the Affected Devices
o Please check your inventory for ClariTEE probes with lot numbers 20250509 and 20250823. Inform ImaCor of the number of applicable probes currently in inventory.
2. Prepare the Products for Return
o Package the affected products securely to prevent damage during shipment.
3. Shipping Instructions
o Please ship the affected products via FedEx using FedEx Account Number 665380920 to cover the shipping cost. Ship to: ImaCor Inc, 50 Jericho Turnpike, Suite 105, Jericho, NY 11753. Destination phone number is (516) 393-0970.
o Attach a copy of this letter inside the package for reference.
4. Replacement Devices
o Once we receive the returned devices, we will ship replacement probes to your facility. Replacement probes are expected to be available on or about October 15, 2024.
Please return all affected devices by October 7. If you have any questions or need assistance, please contact Jenn Kujawski at [email protected]. Our team is ready to assist you with any inquiries and can provide additional details if needed.
Root Cause
Process control
Distribution Pattern
FL ,GA, NJ, TN
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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