Lucid Diagnostics, Inc.: Medical Device Recall in 2024 - (Recall #: Z-1900-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.
Product Description:

Brand Name: EsophaCap Product Name: EsophaCap (25mm diameter, 10 pores/inch) Model/Catalog Number: EC25T10VI Software Version: N/A Product Description: EsophaCap is pouched as individual units. 10 units go into a shelf-box. Component: N/A

Product Classification:

Class II

Date Initiated: April 24, 2024
Date Posted: June 5, 2024
Recall Number: Z-1900-2024
Event ID: 94510
Reason for Recall:

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.

Status: Ongoing
Product Quantity: 220 units (US)
Code Information:

Lot Code: Product sent out to clinical site: Part #: EC25T10VI ; GTIN Number: 00860007510977 ; Lot #'s: 483 (Qty: 120), 502 (Qty: 100) Product at Distributor in Quarantine: Part #: EC25T10VI ; GTIN Number: 00860007510977 ; Lot #'s: 539 (Qty: 99)

Distribution Pattern:

US Nationwide distribution in the states of MN, MD.

Voluntary or Mandated:

Voluntary: Firm initiated