Device recall
Z-2116-2015: Augmentation Kit, Sterile-.Kits containing the Devon Light Glove Catalog…
FDA device recall · Class II · Covidien LLC
Key facts
| Recall number (Z-number) | Z-2116-2015 |
|---|---|
| Recall event | 71113 |
| Product | Augmentation Kit , Sterile-.Kits containing the Devon Light Glove Catalog Number/Description 573732 7620-CWA Augmentation Kit |
| Product code | FSY |
| Recalling firm | Covidien LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 28, 2017 |
| FEI number | 1219930 |
At a glance
- None 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