Device recall
Z-0756-2021: CM 50-001-01 Injectate Kit, accessory device to LiDCOunity v2 Monitor - Product…
FDA device recall · Class II · Lidco Ltd
Key facts
| Recall number (Z-number) | Z-0756-2021 |
|---|---|
| Recall event | 86825 |
| Product | CM 50-001-01 Injectate Kit, accessory device to LiDCOunity v2 Monitor - Product Usage: intended to administer lithium dilution indicator (tube administrative set). |
| Product code | DXG |
| Recalling firm | Lidco Ltd |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 26, 2022 |
| 510(k) numbers | K163334 |
| FEI number | 3001139253 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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