Lucid Diagnostics, Inc. 2024-06-05 Health serious FDA
Health · FDA · Recall #FDA-Z-1900-2024
Brand Name: EsophaCap Product Name: EsophaCap (25mm diameter, 10 pores/inch) … Recall
Issued June 5, 2024 · Lucid Diagnostics, Inc.
In June 2024, Lucid Diagnostics, Inc. recalled the Brand Name: EsophaCap Product Name: EsophaCap (25mm diameter, 10 pores/inch) …, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
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.
What you should do
- 1 Stop using Brand Name: EsophaCap Product Name: EsophaCap (25mm diameter, 10 pores/inch) … right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Lucid Diagnostics, Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Lucid Diagnostics, Inc.
- Category
- Health
- Recall date
- June 5, 2024
- Units affected
- Not reported
- Sold at
- US Nationwide distribution in the states of MN, MD.
- Recall number
- FDA-Z-1900-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- Lucid Diagnostics, Inc. has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.