RecallDepth

ClariTEE Probe- Miniature transesophageal echo ultrasound probe for use with ImaCor ultrasound diagnostic platforms. Model/Catalog Number: CLT-010, CLT-010-1

This recall is currently active, issued October 25, 2024. It was issued by Imacor Inc..

Company
Imacor Inc.
Recall Initiated
September 16, 2024
Posted
October 25, 2024
Recall Number
Z-0231-2025
Quantity
73 units
Firm Location
Jericho, NY
Official Source
View on FDA website ↗

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.

Distribution

FL ,GA, NJ, TN

Lot / Code Info

UDI - Primary - 00861589000108 Lot numbers: 20250509 and 20250823

Root Cause

Process control

Action Taken

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 jenn@imacorinc.com. Our team is ready to assist you with any inquiries and can provide additional details if needed.

More recalls by Imacor Inc.

View all recalls by this company →