Device recall
Z-2302-2018: Flexible Smoothbore Breathing Circuit with Exhalation Port 22mm, Product No…
FDA device recall · Class II · Intersurgical Inc
Key facts
| Recall number (Z-number) | Z-2302-2018 |
|---|---|
| Recall event | 80250 |
| Product | Flexible Smoothbore Breathing Circuit with Exhalation Port 22mm, Product No. 80062000 |
| Product code | CAI |
| Recalling firm | Intersurgical Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 9, 2019 |
| FEI number | 1000120301 |
At a glance
- None Linked 510(k)s
- 1–9 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