RECALL DATABASE

Contact Lens Recall: Pearle Vision 1 day

Announced 2026-09-30 · FDA

CooperVision is recalling Pearle Vision 1 day contact lenses because a small number of lenses in the affected lot are the incorrect power. The recall covers Carton Lot # 11727620152030 and Blister Lot # CB132348, and distribution was nationwide in the US, including MN, OH, and WI. No corrective action is listed in the provided information.

BrandCooperVision, Inc.
ProductBrand Name: Pearle Vision 1 day Product Name: (somofilcon A) Contact Lens Model/Catalog Number: Pearle Vision 1 day
ReasonA small number of lenses within the affected lot are of the incorrect power.
Severitymoderate
Units affected3060
DistributionUS Nationwide distribution in the states of MN, OH, WI.
AgencyFDA

WHAT YOU SHOULD DO

  1. Do not use lenses from the affected lot.
  2. Check your packaging for the listed Carton Lot # 11727620152030 or Blister Lot # CB132348 to determine if yours are affected.
  3. Contact your eye care professional or Pearle Vision for guidance on replacement or disposal.
  4. If you experience vision changes or discomfort, seek medical advice promptly.

How to identify the recalled item

Lot / date codesPearle Vision 1 day; Carton Lot # 11727620152030; Blister Lot # CB132348;
Lot / date codesPearle Vision 1 day; Carton Lot # 11727620152030; Blister Lot # CB132348;

These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.

Other contact lens recalls

See every contact lens recall →

This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.