Device recall
Z-0308-2012: ViroMax viral/bacterial filter. The filter reduces the risk of infection due to…
FDA device recall · Class II · A M Systems Inc
Key facts
| Recall number (Z-number) | Z-0308-2012 |
|---|---|
| Recall event | 55294 |
| Product | ViroMax viral/bacterial filter. The filter reduces the risk of infection due to cross-contamination between patients For use on all patient populations in conjunction with other respiratory devices containing standard 15mm and/or 22mm fittings (such as breathing circuits) to filter respiratory gases… |
| Product code | CAH |
| Recalling firm | A M Systems Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 5, 2012 |
| 510(k) numbers | K063526 |
| FEI number | 3020614 |
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