Recall Ledger

Brand Name: Pearle Vision 1 day Product Name: recall (CooperVision, Inc.)

Medical deviceClass IIOngoing

Summary: CooperVision, Inc. is recalling Brand Name: Pearle Vision 1 day Product Name: (somofilcon A) Contact Lens Model/Catalog Number: Pearle Vision 1 day. Reason: A small number of lenses within the affected lot are of the incorrect power.

What is being recalled

Brand Name: Pearle Vision 1 day Product Name: (somofilcon A) Contact Lens Model/Catalog Number: Pearle Vision 1 day

Why

A small number of lenses within the affected lot are of the incorrect power.

How serious is it

Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.

Where it was sold

US Nationwide distribution in the states of MN, OH, WI. (states named: Minnesota, Ohio, Wisconsin)

How to tell if yours is affected

Pearle Vision 1 day; Carton Lot # 11727620152030; Blister Lot # CB132348;

What to do

Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.

Recall facts

Recall numberZ-3248-2026
CategoryMedical device
AgencyU.S. Food and Drug Administration (FDA)
SeverityClass II
StatusOngoing
Recall startedAugust 12, 2026
ReportedSeptember 30, 2026
CompanyCooperVision, Inc.
Company locationWest Henrietta, NY, United States
Initiated byVoluntary: Firm initiated
Quantity3060

More recalls from CooperVision, Inc. · all medical device recalls · recalls from August 2026

Official FDA record