Device recall
Z-0725-2017: Magnesium on RX Imola analyser IVD
FDA device recall · Class II · Randox Laboratories, Limited
Key facts
| Recall number (Z-number) | Z-0725-2017 |
|---|---|
| Recall event | 75263 |
| Product | Magnesium on RX Imola analyser IVD |
| Product code | JGJ |
| Recalling firm | Randox Laboratories, Limited |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 19, 2017 |
| 510(k) numbers | K052914 |
| FEI number | 1000361607 |
At a glance
- 1–9 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