Device recall
Z-0038-2007: DeVilbiss iFill Personal Oxygen Station model number 535D.
FDA device recall · Class III · Sunrise Medical
Key facts
| Recall number (Z-number) | Z-0038-2007 |
|---|---|
| Recall event | 36174 |
| Product | DeVilbiss iFill Personal Oxygen Station model number 535D. |
| Product code | CAW |
| Recalling firm | Sunrise Medical |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Aug 27, 2009 |
| 510(k) numbers | K053240 |
| FEI number | 2515872 |
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