Device recall
Z-2108-2025: Brand Name: Alcon Laboratories, Inc. Product Name: Constellation Vision System…
FDA device recall · Class II · Alcon Research LLC
Key facts
| Recall number (Z-number) | Z-2108-2025 |
|---|---|
| Recall event | 96832 |
| Product | Brand Name: Alcon Laboratories, Inc. Product Name: Constellation Vision System Vitrectomy Procedure Pak Model/Catalog Number: Many - See 'Attachment 1 - Affected Product List' Software Version: N/A Product Description: Surgical procedure pack to interface with Alcon Constellation Surgical console… |
| Product code | MLZ |
| Recalling firm | Alcon Research LLC |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K141065 |
| FEI number | 1610287 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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