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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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Low RiskFDA Drug
Medications & Supplements/Prescription Drugs

AuroMedics Pharma LLC: Moxifloxacin Ophthalmic Solution Recalled for Discoloration

Agency Publication Date: January 17, 2020
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Summary

AuroMedics Pharma LLC is recalling approximately 100,080 bottles of Moxifloxacin Ophthalmic Solution USP, 0.5%, a prescription antibiotic eye drop used to treat bacterial infections. This recall was initiated after receiving market complaints that the solution inside the bottles had become discolored. Consumers who have these specific eye drops should check their packaging for affected lot numbers and contact their doctor if they have experienced any unusual symptoms.

Risk

The discoloration of the solution indicates a change in the product's physical properties, which may affect the drug's quality or safety when applied to the eye. While the risk level is currently considered low, using a compromised ophthalmic solution could potentially lead to reduced effectiveness or irritation.

What You Should Do

  1. Check your prescription bottle or outer carton of Moxifloxacin Ophthalmic Solution USP, 0.5% (3mL size) for NDC 65862-840-03.
  2. Verify if your bottle belongs to one of the following four affected lots: CMF190008, CMF190009 (Exp. 04/2021), CMF190025, or CMF190026 (Exp. 06/2021).
  3. If your product matches the affected lot numbers, contact your healthcare provider or pharmacist immediately for guidance on an alternative treatment.
  4. Return any unused or discolored product to the pharmacy where it was purchased for a refund.
  5. Contact AuroMedics Pharma LLC at their East Windsor, NJ location or through the contact channels provided on your prescription for further instructions regarding the return process.
  6. For additional questions or to report a problem, call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

💰Full Refund

Refund for unused eye drops.

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: Moxifloxacin Ophthalmic Solution USP, 0.5%, Sterile (3mL Bottle)
Model:
NDC 65862-840-03
Lot Numbers:
CMF190008
CMF190009 (Exp. 04/2021)
CMF190025
CMF190026 (Exp. 06/2021)
Date Ranges: April 2021, June 2021

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 84498
Status: Resolved
Manufacturer: AuroMedics Pharma LLC
Sold By: pharmacies
Manufactured In: India
Units Affected: 100,080 bottles
Distributed To: Nationwide

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 · 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.