Device recall
Z-1201-2014: Mar Cor Purification CWP Reverse Osmosis System. Models 101, 102, 104, and 106.
FDA device recall · Class II · Mar Cor Purification
Key facts
| Recall number (Z-number) | Z-1201-2014 |
|---|---|
| Recall event | 67516 |
| Product | Mar Cor Purification CWP Reverse Osmosis System. Models 101, 102, 104, and 106. |
| Product code | FIP |
| Recalling firm | Mar Cor Purification |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 22, 2014 |
| 510(k) numbers | K974899 |
| FEI number | 3006475063 |
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