Wizcure Pharmaa recalls Vista Gonio Eye Lubricant due to lack of sterility assurance in manufacturing. Products may not be sterile, posing infection risks. Affected lots: all.
Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
Wizcure Pharmaa is recalling all lots of Vista Gonio Eye Lubricant (15ml dry eye relief drops) because they were not made with proper sterility standards. This could lead to eye infections if used.
The product was not manufactured according to current good practices, meaning it might not be sterile. Using non-sterile eye drops can cause infections or other eye issues.
People who own or use the Vista Gonio Eye Lubricant drops are affected. Those with dry eyes or who use eye drops regularly are most at risk.
Check for the product name 'Vista Gonio Eye Lubricant' and the NDC code 77790-022-15. All lots are affected, so no specific batch numbers are needed.
Look for the product name 'Vista Gonio Eye Lubricant' and NDC code 77790-022-15 on the label.
The recall states the product may not be sterile, so it could cause eye infections. Do not use until you get a replacement.
All lots are affected, so no specific batch numbers are needed.
The recall does not specify a remedy, so contact the manufacturer for guidance.
We’ve drafted a message you can send Wizcure Pharmaa to request your refund or repair — edit it as you like.
Subject: Recall D-0349-2026 — Wizcure Pharmaa Wizcure Pharmaa Hello, I own a Wizcure Pharmaa that is covered by recall D-0349-2026 from Wizcure Pharmaa. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
