Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Brand Name: EsophaCap Product Name: EsophaCap (20mm diameter Recalled by Lucid Diagnostics, Inc. Due to The EsophaCap sponge may be at increased risk...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Lucid Diagnostics, Inc. directly.
Affected Products
Brand Name: EsophaCap Product Name: EsophaCap (20mm diameter, 20 pores/inch) Model/Catalog Number: EC20T20VI Software Version: N/A Product Description: EsophaCap is pouched as individual units. 10 units go into a shelf-box. Component: No
Quantity: 157 units (US)
Why Was This Recalled?
The EsophaCap sponge may be at increased risk of detaching from the string during removal of the device from the patient, particularly at the lower esophageal sphincter at the gastroesophageal junction or the upper esophageal sphincter between the pharynx and the esophagus, which is the narrowest part of the alimentary canal.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Lucid Diagnostics, Inc.
Lucid Diagnostics, Inc. has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report