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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

Optase Dry Eye Intense Drops Recalled Due to Lack of Assurance of Sterility

Agency Publication Date: April 28, 2026
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Summary

Scope Health is recalling various lots of Optase Dry Eye Intense Drops (glycerin 0.2%) packaged in 0.33 fl oz bottles. The recall was initiated because the products lack assurance of sterility, meaning the drops might not be free from microorganisms that could cause infection. No injuries or illnesses have been reported to date. These eye drops were sold nationwide through retail pharmacies and optical centers.

Risk

Using non-sterile eye drops can introduce bacteria or other contaminants directly into the eye, potentially leading to serious eye infections or vision loss. Those with compromised immune systems or recent eye surgery are at even higher risk of complications.

What You Should Do

  1. Check your Optase Dry Eye Intense Drops (0.33 fl oz) for the following lot numbers and expiration dates: 8T98 (Exp. 30/04/26), 9T31 (Exp. 30/04/26), 9T32 (Exp. 30/04/26), 2V13 (Exp. 30/06/26), 2V14 (Exp. 30/06/26), 2V15 (Exp. 30/06/26), 3V35 (Exp. 31/08/26), 3V36 (Exp. 30/09/26), 3V37 (Exp. 30/09/26), 5V45 (Exp. 31/03/27), 5V46 (Exp. 31/03/27), 9V12 (Exp. 31/03/27), 1X57 (Exp. 31/05/27), 1X70 (Exp. 31/05/27), and 1X84 (Exp. 31/05/27).
  2. If you have health concerns, contact your healthcare provider or pharmacist.
  3. Return any unused product to the place of purchase for a refund, throw it away, or contact the manufacturer for further instructions.
  4. 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: Optase Dry Eye Intense Drops (Glycerin 0.2%) (0.33 fl oz)
Variants: Glycerin 0.2%, Sterile, Eye Drops
Lot Numbers:
8T98 (Exp. 30/04/26)
9T31 (Exp. 30/04/26)
9T32 (Exp. 30/04/26)
2V13 (Exp. 30/06/26)
2V14 (Exp. 30/06/26)
2V15 (Exp. 30/06/26)
3V35 (Exp. 31/08/26)
3V36 (Exp. 30/09/26)
3V37 (Exp. 30/09/26)
5V45 (Exp. 31/03/27)
5V46 (Exp. 31/03/27)
9V12 (Exp. 31/03/27)
1X57 (Exp. 31/05/27)
1X70 (Exp. 31/05/27)
1X84 (Exp. 31/05/27)
NDC:
72972-002-01

Manufactured for Scope Health Inc.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98802
Status: Active
Manufacturer: SCOPE HEALTH
Sold By: Retail pharmacies; Optical centers
Manufactured In: United States
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.