FDA Device recall Z-3248-2026
Brand Name: Pearle Vision 1 day Product Name: (somofilcon A) Contact Lens Model/Catalog Number: Pearle Vision 1 day
- FDA Device
- Class II
- ongoing
- Published 2026-09-30
On 2026-09-30 the FDA classified a Class II recall of Brand Name: Pearle Vision 1 day Product Name: (somofilcon A) Contact Lens Model/Catalog Number: Pearle Vision 1 day by Coopervision, citing A small number of lenses within the affected lot are of the incorrect power.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3248-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-08-12 |
| Published | 2026-09-30 |
| Last updated | 2026-10-06 05:30 UTC |
| Company | Coopervision |
| Distribution | US |
Product
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.
Identifiers
| code_info | Pearle Vision 1 day; Carton Lot # 11727620152030; Blister Lot # CB132348; |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-10-06 05:30 UTC. Current status: ongoing.
Other recalls by Coopervision
- Sofmed Breathables, (stenfilcon A) contact lens
FDA Device · Class II · 2025-10-01 · Coopervision - Voyant 1-Day Premium Toric, (stenfilcon A) contact lens
FDA Device · Class II · 2025-10-01 · Coopervision - MyDay Toric, stenfilcon A) Contact Lens
FDA Device · Class II · 2025-10-01 · Coopervision - Biofinity XR Toric Contact Lens
FDA Device · Class II · 2025-07-30 · Coopervision - Biofinity Toric Multifocal Contact Lens
FDA Device · Class II · 2025-07-30 · Coopervision
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3248-2026%22
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