Aurobindo Pharma recalls 0.5% moxifloxacin eye drops due to impurities that could cause eye injury. Affected lots from India, expiring June 2023. Stop using immediately.
Failed Impurities/Degradation Specifications
Aurobindo Pharma is recalling certain moxifloxacin eye drops because they may contain impurities that could cause eye injury. This affects specific batches made in India with expiration dates up to June 2023. People with prescriptions for these eye drops should stop using them immediately.
The eye drops may contain impurities that could cause eye injury. This happens because the medication failed to meet purity standards during manufacturing in India.
Prescription holders of the affected moxifloxacin eye drops. People with eye conditions requiring this medication are most at risk.
Check for the 3 mL bottle labeled 'Moxifloxacin Ophthalmic Solution, USP 0.5% w/v, Sterile, Rx Only'. Look for lot numbers CMF210001, CMF210003, or CMF210004 with expiration date June 2023.
Discard the affected eye drops if you have them. Do not use the product.
The eye drops failed impurities and degradation specifications during manufacturing in India.
Lot numbers CMF210001, CMF210003, and CMF210004, expiring June 2023.
Check the label for the 3 mL bottle with the lot numbers mentioned above and expiration date June 2023.
We’ve drafted a message you can send Aurobindo Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0560-2022 — Aurobindo Pharma Aurobindo Pharma Hello, I own a Aurobindo Pharma that is covered by recall D-0560-2022 from Aurobindo Pharma. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
