D-0789-2020 Class III Terminated
FDA drug recall D-0789-2020 was initiated by AuroMedics Pharma LLC on Dec 2, 2019 and is designated Class III. Reason for recall: Discoloration: Market complaints of discoloration in Moxifloxacin Ophthalmic Solution. The recall status is terminated (terminated Nov 22, 2022). Affected quantity: 100,080 bottles.
Recall Details
- Product Type
- Drugs
- Report Date
- Jan 22, 2020
- Initiation Date
- Dec 2, 2019
- Termination Date
- Nov 22, 2022
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 100,080 bottles
Product Description
Moxifloxacin Ophthalmic Solution USP, 0.5%, Sterile, 3mL Bottle, Rx Only, For Topical Ophthalmic Use Only, Distributed by: Aurobindo Pharma USA, Inc., East Windsor, NJ 08520, Made in India, NDC 65862-840-03.
Reason for Recall
Discoloration: Market complaints of discoloration in Moxifloxacin Ophthalmic Solution.
Distribution Pattern
Nationwide in the U.S.
Code Information
Lot #s: CMF190008; CMF190009, Exp. 04/2021; CMF190025; CMF190026, Exp. 06/2021.
Source
- Dataset
- openFDA drug recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for D-0789-2020
- openFDA file date
- Nov 3, 2026
- Loaded by RegDataLab
- Nov 4, 2026