HIGHFDA DRUG

Wizcure Pharmaa Recalls Vista Gonio Eye Lubricant Over Sterility Issues

Wizcure Pharmaa Pvt. Ltd. recalled 139,104 cartons of Vista Gonio Eye Lubricant on December 31, 2025. The recall stems from a lack of assurance of sterility due to non-compliance with manufacturing practices. Consumers are urged to stop using the product immediately and seek guidance from healthcare providers.

Official notice

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DRUG
Recall date
December 31, 2025
Status
ACTIVE
Severity
8/10

Quick Facts at a Glance

Recall Date
December 31, 2025
Hazard Level
HIGH
Brands
VISTA GONIO EYE LUBRICANT, Red Wedding LLC
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

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
VISTA GONIO EYE LUBRICANT, Red Wedding LLC
Product type
Hypromellose Ophthalmic Solution
Model numbers
All lots
UPC codes
77790-022, 77790-022-15
Sold at
Multiple Retailers
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    December 31, 2025

  2. Reported by FDA DRUG

    March 4, 2026

  3. RecallRadar source check

    March 11, 2026

  4. 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 Gonio Eye Lubricant is used to relieve dry eye symptoms. It is commonly purchased by individuals looking for moisture and protection for their eyes.

Why This Is Dangerous

The product's sterility cannot be guaranteed due to manufacturing issues, which increases the risk of eye infections or irritation.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers may experience inconvenience and safety concerns. This recall necessitates immediate action to avoid potential health risks.

Practical Guidance

How to identify if yours is affected

  1. Check if you have Vista Gonio Eye Lubricant in your possession.
  2. Verify the product's NDC: 77790-022-15.
  3. Confirm that the product was purchased after January 1, 2025.

Where to find product info

The NDC and lot numbers can usually be found on the product packaging or label.

What timeline to expect

Refund or replacement processing may take approximately 4-6 weeks.

If the manufacturer is unresponsive

  • Follow up with customer service after 2 weeks.
  • Consider filing a complaint with the FDA if you receive no response.

How to prevent similar issues

  • Look for products with clear sterility certifications.
  • Avoid purchasing eye lubricants from unknown or unverified sources.
  • Check for recent recalls or safety alerts before buying.

Documentation advice

Keep receipts, correspondence, and any documentation related to the recall for your records.

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Product Details

The recalled product is Vista Gonio Eye Lubricant, Hypromellose Ophthalmic Solution USP, 15 ml (1/2 fl. oz.). It was distributed nationwide in the USA. The National Drug Code (NDC) is 77790-022-15.

Key Facts

  • Recall date: December 31, 2025
  • Reported by FDA on March 4, 2026
  • Total quantity recalled: 139,104 cartons
  • Distributed nationwide in the USA

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
All lots
UPC Codes
77790-022
77790-022-15
Affected States
ALL
Report Date
March 4, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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