Device recall
Z-1644-2009: Alcon Vitrectomy 25 GA Custom Pak, Catalog/Item #10240-03, 11077-03, 11187-02…
FDA device recall · Class II · Alcon Laboratories, Inc
Key facts
| Recall number (Z-number) | Z-1644-2009 |
|---|---|
| Recall event | 51964 |
| Product | Alcon Vitrectomy 25 GA Custom Pak, Catalog/Item #10240-03, 11077-03, 11187-02 and 13305-01; distributed by Alcon Laboratories, Inc., Fort Worth, TX 76134. |
| Product code | NGY |
| Recalling firm | Alcon Laboratories, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 14, 2009 |
| 510(k) numbers | K880961 |
| FEI number | 1610287 |
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