FDA Device recall Z-2606-2025
MyDay Toric, stenfilcon A) Contact Lens
- FDA Device
- Class II
- ongoing
- Published 2025-10-01
On 2025-10-01 the FDA classified a Class II recall of MyDay Toric, stenfilcon A) Contact Lens by Coopervision, citing one lot manufactured with an invalid sterilization cycle.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2606-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-08-22 |
| Published | 2025-10-01 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Coopervision |
| Distribution | US |
Product
MyDay Toric, stenfilcon A) Contact Lens. Model/Catalog Number: MyDay Toric. 54% water content, Toric, cast moulded Silicone Hydrogel, In-monomer tinted, contact lens, for Daily Disposable Wear. Blister packaged.
Reason
One lot manufactured with an invalid sterilization cycle.
Identifiers
| code_info | Carton Lot Number: 20735504301008. Blister Lot Number: 6450505898 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2606-2025%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.