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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Drug
Medications & Supplements/Over-the-Counter

Vista and BioGlo Ophthalmic Products Recalled for Lack of Sterility

Agency Publication Date: February 25, 2026
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Summary

Wizcure Pharmaa Private Limited is recalling 418,464 units of various eye drops and diagnostic strips, including Vista Tears, Vista Gel, and BioGlo, due to a lack of assurance of sterility. These products were not manufactured in accordance with current good manufacturing practices, meaning they may be contaminated. The recall affects several products used for dry eye relief and diagnostic eye exams, including polyethylene glycol and hypromellose solutions.

Risk

Non-sterile ophthalmic products intended to be sterile pose a significant risk of eye infections, which could lead to serious injury or permanent vision loss. The manufacturing failures at the facility mean the safety and purity of these products cannot be guaranteed.

What You Should Do

  1. Identify if you have any of the affected Vista or BioGlo products by checking the brand name and packaging details on your eye drop bottles or diagnostic strip boxes.
  2. Check the NDC numbers on your product packaging, which include 77790-001-10, 77790-002-10, 77790-003-10, 77790-022-15, 83851-100-10, 83851-100-30, 17238-900-30, and 17238-900-11.
  3. See the Affected Products section below for the full list of affected codes.
  4. If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact the manufacturer for further instructions.
  5. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Vista Tears Polyethylene Glycol 400 0.4% w/v, Propylene Glycol 0.3% w/v Eye Drops (10 ml)
Variants: Lubricant Drops, Dry Eye Relief
Lot Numbers:
All lots
NDC:
77790-001-10

Recall #: D-0346-2026; Manufactured for and distributed by hi-health.

Product: Vista Gel Hypromellose USP 0.3% w/v Eye Drops (10 ml)
Variants: Lubricating Gel, Dry Eye Relief
Lot Numbers:
All lots
NDC:
77790-002-10

Recall #: D-0347-2026; Manufactured for and distributed by hi-health.

Product: Vista Meibo Tears Propylene Glycol 0.6% w/v Eye Drops (10 ml)
Variants: Advanced Dry Eye Relief, Revitalizing Formula
Lot Numbers:
All lots
NDC:
77790-003-10

Recall #: D-0348-2026; Manufactured for and distributed by hi-health.

Product: Vista Gonio Eye Lubricant, Hypromellose Ophthalmic Solution USP (15 ml)
Variants: Sterile Drops, Dry Eye Relief
Lot Numbers:
All lots
NDC:
77790-022-15

Recall #: D-0349-2026; Manufactured for and distributed by hi-health.

Product: CHNaO Fluorescein Sodium Ophthalmic Strips, USP 1mg
Variants: 100-count box, 300-count box
Lot Numbers:
All lots
NDC:
83851-100-10
83851-100-30

Recall #: D-0350-2026; Distributed by Vistamerica USA.

Product: Bio Glo Fluorescein Sodium Ophthalmic Strips USP (300 strips)
Variants: Diagnostic strips
Lot Numbers:
All lots
NDC:
17238-900-30

Recall #: D-0351-2026; Manufactured for & distributed by HUB Pharmaceuticals, LLC.

Product: BioGlo Fluorescein Sodium Ophthalmic Strips USP (100 strips)
Variants: Diagnostic strips
Lot Numbers:
All lots
NDC:
17238-900-11

Recall #: D-0352-2026; Manufactured for & distributed by HUB Pharmaceuticals, LLC.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98253
Status: Active
Manufacturer: Wizcure Pharmaa Private Limited
Sold By: hi-health; Vistamerica USA; HUB Pharmaceuticals, LLC
Manufactured In: India
Units Affected: 7 products (5,760 cartons; 17,280 cartons; 11,520 cartons; 139,104 cartons; 10,080 boxes; 50,400 Boxes; 184,320 containers)
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.