HIGH

Wizcure Pharmaa Recalls Vista Gel Eye Drops Due to Sterility Issues

Wizcure Pharmaa recalled 17,280 cartons of Vista Gel Hypromellose eye drops on December 31, 2025. The recall stems from a lack of assurance of sterility, raising potential health risks for users. Consumers should stop using the product immediately and contact their healthcare provider for guidance.

Quick Facts at a Glance

Recall Date
December 31, 2025
Hazard Level
HIGH
Brands
VISTA HYPROMELLOSE DRY EYE RELIEF, Red Wedding LLC
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

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

Get instant alerts for Health & Personal Care recalls

Be the first to know. Free instant alerts to your inbox.

No spamUnsubscribe anytime

About This Product

Vista Gel Hypromellose is a lubricating eye drop used to relieve dry eye symptoms. It is popular among consumers seeking relief from discomfort caused by environmental factors such as wind, smoke, or prolonged screen time.

Why This Is Dangerous

The lack of assurance of sterility indicates that the product may be contaminated, posing a risk of infection to users.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers who rely on these eye drops for dry eye relief may face health risks due to potential contamination. The recall creates inconvenience as users must find alternative treatments.

Practical Guidance

How to identify if yours is affected

  1. Check the product label for the brand name 'Vista Gel Hypromellose'.
  2. Verify the product size (10 ml) and check if it is in the recalled lots.
  3. If unsure, consult your healthcare provider for assistance.

Where to find product info

The serial number and lot information can typically be found on the packaging or label of the product.

What timeline to expect

Expect a refund or replacement processing time of approximately 4-6 weeks.

If the manufacturer is unresponsive

  • Contact the retailer for follow-up on your refund request.
  • Document your communication attempts and escalate to the FDA if necessary.

How to prevent similar issues

  • Always check for recalls on over-the-counter medications.
  • Look for products with clear sterilization and manufacturing practices.
  • Consult a healthcare provider for recommendations on safe eye drop alternatives.

Documentation advice

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

Product Details

The recalled product is Vista Gel Hypromellose USP 0.3% w/v, Eye Drops Dry Eye Relief Lubricating Gel, 10 ml. It is manufactured by Wizcure Pharmaa PVT. LTD in India and distributed by hi-health in Scottsdale, AZ. All lots of this product are affected.

Key Facts

  • Recall date: December 31, 2025
  • Reported date: March 4, 2026
  • Quantity recalled: 17,280 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

Get Alerts for Health & Personal Care Recalls

Get instant alerts for recalls that affect you. Free forever.

Safety Assessment

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

Product Details

Model Numbers
All lots
UPC Codes
77790-002
77790-002-10
Affected States
ALL
Report Date
March 4, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

Related Recalls

Vehicles & Parts
HIGH

Mazda CX-70 Recall 2025 for Powertrain Control Module Software May Lose Drive Power

Mazda North American Operations is recalling 2024 CX-90 and 2025 CX-70 SUVs sold through Mazda dealers. The PCM and ECM software can illuminate malfunction indicator lights and cause a loss of drive power, increasing crash risk. Owner notification letters were mailed December 19, 2024, and Mazda will reprogram the PCM and ECM at no charge.

Mazda
Loss of
Read more
Vehicles & Parts
HIGH

Nissan Kicks 2025 Certification Label Recall for GVWR/GAWR Errors (PD136, PMA47)

Nissan North America is recalling certain 2025 Nissan Kicks vehicles sold through Nissan dealers nationwide. The certification label may print incorrect GVWR and GAWR values, risking overload. Some SR trims with a 19-inch wheel package may display an incorrect wheel size on the label, and owners should contact their Nissan dealer to arrange replacement labels.

Nissan
An overloaded
Read more