FDA Device recall Z-0529-2015
Soft Contact Lens
- FDA Device
- Class II
- terminated
- Published 2014-12-17
On 2014-12-17 the FDA classified a Class II recall of Soft Contact Lens by Cooper Vision Caribbean, citing portions of the lots may contain units with an incorrect lens axis condition.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0529-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-10-28 |
| Published | 2014-12-17 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Cooper Vision Caribbean |
| Distribution | US |
Product
Soft Contact Lens
Reason
Portions of the lots may contain units with an incorrect lens axis condition.
Identifiers
| code_info | Lots # 8246525202 & 8255525096 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0529-2015%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.