Device recall
Z-0305-2026: Brand Name: Alcon Laboratories, Inc. Product Name: Accessory devices for Unity…
FDA device recall · Class II · Alcon Research LLC
Key facts
| Recall number (Z-number) | Z-0305-2026 |
|---|---|
| Recall event | 97415 |
| Product | Brand Name: Alcon Laboratories, Inc. Product Name: Accessory devices for Unity and Constellation surgical consoles Model/Catalog Number: Many - See 'Attachment 1 - Affected Product List' 8065750918 PAK,I/A LINE,NGVS 8065750957 ASSY,SHIP,CONSTELLATION VFC 8065750972 ENDOILLUMATOR,RFID,23G 8065751014… |
| Product code | HQC |
| Recalling firm | Alcon Research LLC |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K141065, K233876, K242184 |
| 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