[Recalled] AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual correction of aphakia in adult patients. Tecnis CL Mono 13 mm with the following diopter sizes: 18.5-19.0
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual correction of aphakia in adult patients. Tecnis CL Mono 13 mm with the following diopter sizes: 18.5-19.0 Product Usage: AMO TECNIS CL monofocal foldable IOLs with OptiEdge de |
|---|---|
| Brand / manufacturer | AMO Puerto Rico Manufacturing, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2280-2014 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 13 May 2014 |
| EAN / barcode | 1001141312 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Units may be labeled with the incorrect diopter power.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from AMO Puerto Rico Manufacturing, Inc.
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.