Device recall
Z-1068-05: Sequoia Oxymatic electronic oxygen conservers. Models OM-302, OM-311 ***and…
FDA device recall · Class II · Chad Therapeutics Inc
Key facts
| Recall number (Z-number) | Z-1068-05 |
|---|---|
| Recall event | 31611 |
| Product | Sequoia Oxymatic electronic oxygen conservers. Models OM-302, OM-311 ***and OM-312***. |
| Product code | BZD |
| Recalling firm | Chad Therapeutics Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 30, 2006 |
| 510(k) numbers | K000890, K003455 |
| FEI number | 2024040 |
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