Device recall
Z-1898-2012: Adult Divided Cannula end tidal C)2 sampling w/male luer-lock connector. 7 ft…
FDA device recall · Class II · SALTER LABS
Key facts
| Recall number (Z-number) | Z-1898-2012 |
|---|---|
| Recall event | 62272 |
| Product | Adult Divided Cannula end tidal C)2 sampling w/male luer-lock connector. 7 ft, oxygen tube, 7 ft. CO2 tube RX only.For Single Patient Use only. Distributed by Tri-Anium Assembled in Mexico. Usage: Delivery of Anesthesia. |
| Product code | CCK |
| Recalling firm | SALTER LABS |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 27, 2012 |
| 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