Device recall
Z-0759-2020: CARESCAPE Respiratory Module E-sCAiOVE
FDA device recall · Class I · GE Healthcare, LLC
Key facts
| Recall number (Z-number) | Z-0759-2020 |
|---|---|
| Recall event | 84034 |
| Product | CARESCAPE Respiratory Module E-sCAiOVE |
| Product code | CCK |
| Recalling firm | GE Healthcare, LLC |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Sep 26, 2023 |
| FEI number | 2126677 |
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