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.
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.
You have 2 options:
Recall #: D-0346-2026; Manufactured for and distributed by hi-health.
Recall #: D-0347-2026; Manufactured for and distributed by hi-health.
Recall #: D-0348-2026; Manufactured for and distributed by hi-health.
Recall #: D-0349-2026; Manufactured for and distributed by hi-health.
Recall #: D-0350-2026; Distributed by Vistamerica USA.
Recall #: D-0351-2026; Manufactured for & distributed by HUB Pharmaceuticals, LLC.
Recall #: D-0352-2026; Manufactured for & distributed by HUB Pharmaceuticals, LLC.
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.
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.