Device recall
Z-1829-2019: EGIA 60 ARTICULATING MED THICK SULU, EGIA60AMT
FDA device recall · Class II · Covidien LLC
Key facts
| Recall number (Z-number) | Z-1829-2019 |
|---|---|
| Recall event | 82950 |
| Product | EGIA 60 ARTICULATING MED THICK SULU , EGIA60AMT |
| Product code | GDW |
| Recalling firm | Covidien LLC |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K111825, K160176 |
| FEI number | 1219930 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 Products in the same recall event
- 100–999 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