Device recall
Z-0694-2020: TEKIA Model 872 Single Piece Hydrophilic Acrylic Intraocular Lenses, Diopter…
FDA device recall · Class II · Tekia, Inc.
Key facts
| Recall number (Z-number) | Z-0694-2020 |
|---|---|
| Recall event | 83903 |
| Product | TEKIA Model 872 Single Piece Hydrophilic Acrylic Intraocular Lenses, Diopter 15.0, Sterile. The firm name on the label is TEKIA, INC., Irvine, CA. |
| Product code | HQL |
| Recalling firm | Tekia, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 16, 2020 |
| FEI number | 3002023310 |
At a glance
- None 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