Quick Facts at a Glance
- Recall Date
- December 31, 2025
- Hazard Level
- HIGH
- Brand
- Wizcure Pharmaa Private
- Category
- Health & Personal Care
- Sold At
- Multiple Retailers
- Geographic Scope
- 1 states
- At-Risk Groups
- GENERAL
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- Wizcure Pharmaa Private
- Product type
- Eye Drops
- Model numbers
- All lots
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
December 31, 2025
Reported by FDA DRUG
March 4, 2026
RecallRadar source check
March 11, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
What You Should Do
Consumers and healthcare providers should stop using this product immediately. Contact Wizcure Pharmaa Private Limited or your healthcare provider for guidance. Notification method: Letter
About This Product
Vista Tears Eye Drops are intended for dry eye relief and lubrication. Consumers typically purchase these drops to alleviate discomfort caused by dryness or irritation in the eyes.
Industry Context
This recall is not part of a broader industry pattern.
Practical Guidance
How to identify if yours is affected
- Check the product label for the name 'Vista Tears' and the manufacturing details.
- Verify if your product is the 10 ml size with the NDC 77790-001-10.
- Look for any recalls listed on the FDA website.
Where to find product info
The NDC number and manufacturing details are usually found on the product packaging or label.
What timeline to expect
Expect a refund or replacement process to take approximately 4-6 weeks.
If the manufacturer is unresponsive
- Document all communications with the retailer or manufacturer.
- Consider reaching out to the FDA for guidance on further actions.
How to prevent similar issues
- Look for eye drops with clear labeling of sterility assurance.
- Consider purchasing from reputable brands with strong safety records.
- Check for recent recalls before purchasing health products.
Documentation advice
Keep records of your purchase, including receipts and any correspondence related to the recall.
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Product Details
The recalled product is Vista Tears Polyethylene Glycol 400 0.4% w/v and Propylene Glycol 0.3% w/v Eye Drops. The product is packaged in 10 ml (1/3 fl. oz.) bottles. It was manufactured by Omni Lens Pvt. Ltd. and distributed by hi-health.
Key Facts
- 5,760 cartons recalled nationwide
- Lack of sterility assurance
- Distributed by hi-health in Scottsdale, AZ
- Contact healthcare provider for guidance
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Safety Guide
Not sure what to do next? Our guide walks you through the process step by step.
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