FDA Device recall Z-2153-2021
FRESH DAY 1 DAY TORIC Power -07.00 -1.25/010 Daily Disposable Contact Lens with UV blocker
- FDA Device
- Class II
- terminated
- Published 2021-08-04
On 2021-08-04 the FDA classified a Class II recall of FRESH DAY 1 DAY TORIC Power -07.00 -1.25/010 Daily Disposable Contact Lens with UV blocker by Coopervision, citing misaligned placement of an axis mark can cause the patient to experience blurred vision.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2153-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-05-19 |
| Published | 2021-08-04 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Coopervision |
| Distribution | US |
Product
FRESH DAY 1 DAY TORIC Power -07.00 -1.25/010 Daily Disposable Contact Lens with UV blocker
Reason
Misaligned placement of an axis mark can cause the patient to experience blurred vision
Identifiers
| code_info | Lot Number: W0106186 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Other recalls by Coopervision
- Brand Name: Pearle Vision 1 day Product Name: (somofilcon A) Contact Lens Model/Catalog Number: Pearle Vision 1 day
FDA Device · Class II · 2026-09-30 · 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
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2153-2021%22
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