FDA Drug recall D-0349-2026
Vista Gonio Eye Lubricant, Hypromellose Ophthalmic Solution USP (Sterile Drops
- FDA Drug
- Class II
- ongoing
- Published 2026-03-04
On 2026-03-04 the FDA classified a Class II recall of Vista Gonio Eye Lubricant, Hypromellose Ophthalmic Solution USP (Sterile Drops by Wizcure Pharmaa Private, citing lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0349-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-12-31 |
| Published | 2026-03-04 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Wizcure Pharmaa Private |
| Distribution | US |
Product
Vista Gonio Eye Lubricant, Hypromellose Ophthalmic Solution USP (Sterile Drops. Dry Eye Relief, 15 ml. (1/2 fl. oz.), Wizcure Pharmaa Pvt. Ltd., H-881, Phase-3, RIICO Industrial Area, Bhiwadi-901019, INDIA, Manufactured for and distributed by: hi-health, 15207 N. 75th Street, Suite #104, Scottsdale, AZ, 85260, NDC 77790-022-15.
Reason
Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
Identifiers
| ndc | 77790-022-15 |
|---|---|
| code_info | All lots |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0349-2026%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.