Lucid Diagnostics recalls

Lucid Diagnostics has 2 recalls on record with the FDA and USDA, the earliest in 2024 and the latest reported on 5 Jun 2024. 2 are still ongoing. The most frequent reason is device malfunction.

Total recalls2since 2024

Last 12 months0reported

Class I00% of total

Ongoing2latest 5 Jun 2024

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 2 100%Class III 0 0%

Why lucid diagnostics is recalled

Device Malfunction2100%

Product types

Medical Software2100%

By year

20242100%

Ongoing lucid diagnostics recalls

2 active

Reported	Class	Recall	Company	Reason	Where
5 Jun 2024Device	CLASS II	EsophaCap diameter, 20 pores/inch) recalled by Lucid Diagnostics	Lucid Diagnostics	Device Malfunction	Nationwide
5 Jun 2024Device	CLASS II	EsophaCap diameter, 10 pores/inch) recalled by Lucid Diagnostics	Lucid Diagnostics	Device Malfunction	Nationwide

All lucid diagnostics recalls, newest first

2 total

Reported	Class	Recall	Company	Reason	Where
5 Jun 2024Device	CLASS II	EsophaCap diameter, 20 pores/inch) recalled by Lucid Diagnostics	Lucid Diagnostics	Device Malfunction	Nationwide
5 Jun 2024Device	CLASS II	EsophaCap diameter, 10 pores/inch) recalled by Lucid Diagnostics	Lucid Diagnostics	Device Malfunction	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.