Wizcure Pharmaa recalls Vista Tears eye drops due to lack of sterility assurance. Products may not be safe for use as they were not manufactured per current good practices.
Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
Wizcure Pharmaa is recalling Vista Tears eye drops because they were not made with proper sterility standards. This could mean the drops might cause infections or other health issues if used.
The eye drops were not manufactured according to current good practices, which means they might not be sterile. This could lead to eye infections or other health problems if used.
People who own or use Vista Tears eye drops from this recall. Those with dry eyes or needing lubricant drops are most at risk.
Check for the product name 'Vista Tears Polyethylene Glycol 400 0.4% w/v, Propylene Glycol 0.3% w/v Eye Drops' on the label. The product was manufactured by Omni Lens Pvt. Ltd. in Ahmedabad, India, and distributed by hi-health in Scottsdale, Arizona.
Look for the product name and manufacturer details on the label to confirm if it's part of this recall.
The eye drops were not manufactured in conformance with current good manufacturing practices, which means they may not be sterile.
The recall record does not specify a remedy, so check the product label to see if it's affected and contact the manufacturer for further instructions.
The recall states a lack of sterility assurance, which could lead to infections, but the record does not mention a risk of serious injury in normal use.
We’ve drafted a message you can send Wizcure Pharmaa to request your refund or repair — edit it as you like.
Subject: Recall D-0346-2026 — Wizcure Pharmaa Wizcure Pharmaa Hello, I own a Wizcure Pharmaa that is covered by recall D-0346-2026 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.
