Device recall
Z-2009-2009: Cobham AMOGS Advanced Medical Oxygen Generating System, 70309-03900-101…
FDA device recall · Class II · Carleton Life Support Systems Inc
Key facts
| Recall number (Z-number) | Z-2009-2009 |
|---|---|
| Recall event | 52766 |
| Product | Cobham AMOGS Advanced Medical Oxygen Generating System, 70309-03900-101. Concentrator, Oxygen, Molecular Sieve, S/A P/N: 70309-03900-101, Mfg P/N 3261165-0101. The firm name on the label is Carleton Life Support Systems Inc., Davenport, IA. |
| Product code | CAW |
| Recalling firm | Carleton Life Support Systems Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 22, 2012 |
| 510(k) numbers | K082829 |
| FEI number | 3002840531 |
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