Device recall
Z-2470-2012: This voluntary medical device correction is related to Alcon products that…
FDA device recall · Class II · Alcon Research, LTD.
Key facts
| Recall number (Z-number) | Z-2470-2012 |
|---|---|
| Recall event | 62419 |
| Product | This voluntary medical device correction is related to Alcon products that present a 23G nonvalved trocar cannula and infusion cannula together. These items are available as components within Accurus 23G TotalPLUS Pak, Accurus 23G Combined Procedure Packs (0.9mm and 1.1mm), Constellation 23G Total… |
| Product code | NGY |
| Recalling firm | Alcon Research, LTD. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 12, 2013 |
| FEI number | 1000117501 |
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