Device recall
Z-2856-2016: TECNIS Multifocal 1-Piece Intraocular Lens, Model No. ZKB00, ZLB00; The product…
FDA device recall · Class II · Abbott Medical Optics Inc. (AMO)
Key facts
| Recall number (Z-number) | Z-2856-2016 |
|---|---|
| Recall event | 75051 |
| Product | TECNIS Multifocal 1-Piece Intraocular Lens, Model No. ZKB00, ZLB00; The product is indicated for primary implantation for the visual correction of aphakia in adult patients with and without presbyopia in whom a cataractous lens has been removed by extracapsular cataract extraction and who desire… |
| Product code | HQL |
| Recalling firm | Abbott Medical Optics Inc. (AMO) |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 23, 2016 |
| PMA numbers | P980040 |
| FEI number | 3003843509 |
At a glance
- None 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