Device recall
Z-0230-2016: Inspiration Ventilator System, i Series and LS 12.1 LCD. The Inspiration 7i / 5i…
FDA device recall · Class I · Event Medical LTD
Key facts
| Recall number (Z-number) | Z-0230-2016 |
|---|---|
| Recall event | 72491 |
| Product | Inspiration Ventilator System, i Series and LS 12.1 LCD. The Inspiration 7i / 5i Ventilator System is to be used by healthcare professionals in hospitals or healthcare facilities and intra-hospital transport. |
| Product code | CBK |
| Recalling firm | Event Medical LTD |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jun 22, 2017 |
| 510(k) numbers | K130178 |
| FEI number | 3006135941 |
At a glance
- 1–9 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