Device recall
Z-1929-2010: Constellation Vision System, Model: Constellation LXT, Catalogue Number…
FDA device recall · Class I · Alcon Research LTD dba Alcon Laboratories, Inc.
Key facts
| Recall number (Z-number) | Z-1929-2010 |
|---|---|
| Recall event | 55648 |
| Product | Constellation Vision System, Model: Constellation LXT, Catalogue Number: 8065751550 The Constellation Vision System is an ophthalmic microsurgical system that is indicated for both anterior segment (i.e. phacoemulsification and removal of cataracts) and posterior segment (i.e., vitreoretinal)… |
| Product code | HQC |
| Recalling firm | Alcon Research LTD dba Alcon Laboratories, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Sep 19, 2011 |
| 510(k) numbers | K063583 |
| FEI number | 1000125771 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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