Device recall
Z-0705-2018: Rusch Greenlite MAC 1, Catalog Number 004551001. Used during tracheal…
FDA device recall · Class II · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-0705-2018 |
|---|---|
| Recall event | 78929 |
| Product | Rusch Greenlite MAC 1, Catalog Number 004551001. Used during tracheal intubation. |
| Product code | CCW |
| Recalling firm | Teleflex Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 13, 2021 |
| FEI number | 3005747797 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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