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.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2153-2021%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.