Device recall
Z-1899-2024: Brand Name: EsophaCap Product Name: EsophaCap (20mm diameter, 20 pores/inch)…
FDA device recall · Class II · Lucid Diagnostics, Inc.
Key facts
| Recall number (Z-number) | Z-1899-2024 |
|---|---|
| Recall event | 94510 |
| Product | 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 |
| Product code | EOX |
| Recalling firm | Lucid Diagnostics, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K203450 |
| FEI number | 3016490370 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database