Device recall
Z-2242-2011: Salter Labs Nasal Cannula (Adult) Salter Style with 14' (4.3) supply tube…
FDA device recall · Class II · Salter Laboratories, Division of Regulatory Affairs
Key facts
| Recall number (Z-number) | Z-2242-2011 |
|---|---|
| Recall event | 58564 |
| Product | Salter Labs Nasal Cannula (Adult) Salter Style with 14' (4.3) supply tube. Single Patient use. Do not sterilize. Used to deliver supplemental oxygen or airflow to a patient or person in need of respiratory help. |
| Product code | CCK |
| Recalling firm | Salter Laboratories, Division of Regulatory Affairs |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 23, 2011 |
| FEI number | 1314417 |
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