Device recall
Z-0930-03: Rejuv O2 Home Oxygen Spa 98% + Pure, Non-pressurized Oxygen for Breathing…
FDA device recall · Class II · System 02 Inc
Key facts
| Recall number (Z-number) | Z-0930-03 |
|---|---|
| Recall event | 26198 |
| Product | Rejuv O2 Home Oxygen Spa 98% + Pure, Non-pressurized Oxygen for Breathing. Benefits of Oxygen Therapy May Include: Increased Energy, Increased Mental Alertness, Increased Concentration and Memory, Increased Stamina, Improved Sleep, Relief of Stress and Anxiety. Portable Oxygen Delivery System: 98%+… |
| Product code | CAW |
| Recalling firm | System 02 Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 20, 2008 |
| FEI number | 3003038637 |
At a glance
- None 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