CooperVision, Inc.: Medical Device Recall in 2025 - (Recall #: Z-2606-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: August 22, 2025

Date Posted: October 1, 2025

Recall Number: Z-2606-2025

Event ID: 97515

Reason for Recall:

One lot manufactured with an invalid sterilization cycle.

Status: Ongoing

Product Quantity: 4,140 units

Code Information:

Carton Lot Number: 20735504301008. Blister Lot Number: 6450505898

Distribution Pattern:

US Nationwide distribution in the states of Florida, Kentucky, North Carolina, and Wisconsin.

Voluntary or Mandated:

Voluntary: Firm initiated