Device recall
Z-0961-05: Portex HEPA Bacterial /Viral Filter, Non-Latex Ref: 002890
FDA device recall · Class II · Smiths Medical International Ltd
Key facts
| Recall number (Z-number) | Z-0961-05 |
|---|---|
| Recall event | 32297 |
| Product | Portex HEPA Bacterial /Viral Filter, Non-Latex Ref: 002890 |
| Product code | CAH |
| Recalling firm | Smiths Medical International Ltd |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 8, 2012 |
| 510(k) numbers | K930816 |
| FEI number | 3002807908 |
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