Device recall
Z-2950-2026: EndoFLIP System that includes: ENDOFLIP 1 SYSTEM EF-100 05391530810050…
FDA device recall · Class II · Covidien, LLC
Key facts
| Recall number (Z-number) | Z-2950-2026 |
|---|---|
| Recall event | 99176 |
| Product | EndoFLIP System that includes: ENDOFLIP 1 SYSTEM EF-100 05391530810050 10884521809307 REFURBISHED SYSTEM RFG-EF100 ENDOFLIP 1 10884521808096 05391530810166 DL ENDOFLIP 1 10884521786684 |
| Product code | FFX |
| Recalling firm | Covidien, LLC |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K183072 |
| FEI number | 3004904811 |
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