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ImaCor Inc. recalls ClariTEE Probe- Miniature transesophageal echo ultrasound probe for use with ImaCor ultrasound diagnostic platforms. Mo
Recalled November 6, 2024 · FDA recall Z-0231-2025 · ImaCor
Hazard
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. · FDA Class II
Units
73 units
Sold at
FL ,GA, NJ, TN
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 impact on the quality of images obtained from the probes.
Product
ClariTEE Probe- Miniature transesophageal echo ultrasound probe for use with ImaCor ultrasound diagnostic platforms. Model/Catalog Number: CLT-010, CLT-010-1
Manufacturer(s)
ImaCor Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →