- Recalling firm
- CooperVision, Inc.
- Reason for recall
- A small number of lenses within the affected lot are of the incorrect power.
- Affected products (lot / model / serial)
- Pearle Vision 1 day; Carton Lot # 11727620152030; Blister Lot # CB132348;
- Units affected
- 3060
- Distribution pattern
- US Nationwide distribution in the states of MN, OH, WI.
- Firm location
- West Henrietta, NY, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-3248-2026
- Recall initiated
- August 12, 2026
- FDA classification date
- September 18, 2026
- FDA report date
- September 30, 2026
- FDA event ID
- 99766
- Last updated on HTM Vibe
- October 6, 2026
