Device recall
Z-1824-2018: Covidien" Best Practices" Procedure Kits containing Auto Suture" Endo GIA"…
FDA device recall · Class II · COVIDIEN MEDTRONIC
Key facts
| Recall number (Z-number) | Z-1824-2018 |
|---|---|
| Recall event | 79974 |
| Product | Covidien" Best Practices" Procedure Kits containing Auto Suture" Endo GIA" Devices Product Usage: The Endo GIA universal and Endo GIA universal XL staplers place two, triple-staggered rows of titanium staples and simultaneously divides the tissue between the two, triple-staggered rows. The size of… |
| Product code | GDW |
| Recalling firm | COVIDIEN MEDTRONIC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 17, 2020 |
| 510(k) numbers | K111825 |
| 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