FDA Device recall Z-1282-2023
Clariti 1-day toric soft contact lenses, Power -1.00 -1.25/90
- FDA Device
- Class II
- ongoing
- Published 2023-03-29
On 2023-03-29 the FDA classified a Class II recall of Clariti 1-day toric soft contact lenses, Power -1.00 -1.25/90 by Coopervision, citing the lenses manufactured in the affected lot were made with a misaligned axis resulting in lenses with the incorrect power.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1282-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-02-14 |
| Published | 2023-03-29 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Coopervision |
| Distribution | US |
Product
Clariti 1-day toric soft contact lenses, Power -1.00 -1.25/90
Reason
The lenses manufactured in the affected lot were made with a misaligned axis resulting in lenses with the incorrect power.
Identifiers
| code_info | Lot Number W0124677 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1282-2023%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.