Device recall
Z-0175-2022: Cliquid MD version 3.4 software used in conjunction with Analyst MD software on…
FDA device recall · Class II · AB SCIEX
Key facts
| Recall number (Z-number) | Z-0175-2022 |
|---|---|
| Recall event | 88748 |
| Product | Cliquid MD version 3.4 software used in conjunction with Analyst MD software on SCIEX Citrine & 4500MD series liquid chromatography-tandem mass spectrometry (LC-MS/MS) systems. Model No. 5088288 |
| Product code | DOP |
| Recalling firm | AB SCIEX |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 23, 2024 |
| FEI number | 3008336863 |
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