Warning
Wizcure Pharmaa Private Limited Recalls Vista Gonio Eye Lubricant
This is a Class II recall. This product may cause temporary health problems or pose a slight threat of a serious nature.
Source: FDA
WarningRecall #D-0349-2026Drug / Pharmaceutical
Wizcure Pharmaa Private Limited Recalls Vista Gonio Eye Lubricant
Wizcure Pharmaa Private Limited · Class II — Moderate Risk
Product Description
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 for Recall
Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
FDA Classification
Class II — Moderate Risk
A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Distribution
Distributed Nationwide in the USA
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
The FDA classified this recall as Class II, indicating the pharmaceutical product may cause temporary health problems or poses a slight threat of a serious nature. Wizcure Pharmaa Private Limited initiated the recall on December 31, 2025 affecting 139,104 cartons. Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices. The product was distributed in Distributed Nationwide in the USA. Consumers should check their purchases and discontinue use of any affected product. Contact Wizcure Pharmaa Private Limited for further instructions.
Sources: FDA openFDA Enforcement Database
This recall appears in: Drug & Medication Defects.