Device recall
Z-2237-2011: Nasal Cannula (Adult) Salter Style with modified nasal prongs, 7" (2.1M) Q…
FDA device recall · Class II · Salter Laboratories, Division of Regulatory Affairs
Key facts
| Recall number (Z-number) | Z-2237-2011 |
|---|---|
| Recall event | 58563 |
| Product | Nasal Cannula (Adult) Salter Style with modified nasal prongs, 7" (2.1M) Q supply tube and CO2 sample tube with male luer connector 22mm (I.D) x 6mm (O.D) Adaptor. Adult Divided Cannula. Single Patient Use. Do not Sterilize Salter Labs, 100 W. Sycamore Road, Arvin, CA 93293 Used to deliver… |
| Product code | CCK |
| Recalling firm | Salter Laboratories, Division of Regulatory Affairs |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 23, 2011 |
| 510(k) numbers | K892406 |
| FEI number | 1314417 |
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