FDA Device recall Z-1865-2021
ACUVUE VITA soft (hydrophilic) contact lens (spherical) for daily wear
- FDA Device
- Class II
- terminated
- Published 2021-06-23
On 2021-06-23 the FDA classified a Class II recall of ACUVUE VITA soft (hydrophilic) contact lens (spherical) for daily wear by Johnson And Johnson Vision Care, citing potential that a limited number of individual contact lens packages have an incomplete packaging seal.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1865-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-05-06 |
| Published | 2021-06-23 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Johnson And Johnson Vision Care |
| Distribution | US |
Product
ACUVUE VITA soft (hydrophilic) contact lens (spherical) for daily wear. Base Curve 8.8, Refractive Power -1.50
Reason
Potential that a limited number of individual contact lens packages have an incomplete packaging seal.
Identifiers
| upc | 733905989612 |
|---|---|
| code_info | UPC 733905989612 LOT # BOOWWWL |
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-1865-2021%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.