Device recall
Z-0365-2017: Covidien Devon Light Glove sub-assembly non-sterile For Kit Packers Product…
FDA device recall · Class II · Covidien LLC
Key facts
| Recall number (Z-number) | Z-0365-2017 |
|---|---|
| Recall event | 75302 |
| Product | Covidien Devon Light Glove sub-assembly non-sterile For Kit Packers Product Usage: A disposable, sterile, single-use cover for compatible surgical light handles |
| Product code | LRO |
| Recalling firm | Covidien LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 5, 2019 |
| FEI number | 1219930 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1,000+ 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