FDA Device recall Z-2270-2024
24K Premium Lense, Distributed by Updream Inc
- FDA Device
- Class II
- ongoing
- Published 2024-07-17
On 2024-07-17 the FDA classified a Class II recall of 24K Premium Lense, Distributed by Updream Inc by Ontact, citing contact lenses recalled due to potential bacterial contamination.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2270-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-03-20 |
| Published | 2024-07-17 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Ontact |
| Distribution | US |
Product
24K Premium Lense, Distributed by Updream Inc.
Reason
Contact lenses recalled due to potential bacterial contamination.
Identifiers
| code_info | All distributed lenses. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2270-2024%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.