Akorn recalls sterile lubricant eye ointment due to CGMP deviations. Check NDC 17478-062-35 and expiration dates for affected lots. No specific remedy stated in recall notice.
CGMP Deviations:
Akorn is recalling sterile lubricant eye ointment tubes that were manufactured with CGMP deviations. This recall does not specify a remedy or safety risk that requires immediate action.
The recall mentions CGMP deviations, which are regulatory violations in manufacturing processes. However, the record does not explain what these deviations are or how they could affect product safety.
People who own or use the recalled lubricant eye ointment tubes. Those with the specific NDC code and expiration dates listed are most at risk.
Check for the NDC code 17478-062-35 on the tube. The product was manufactured with specific expiration dates listed in the recall notice.
Look for the NDC code 17478-062-35 and expiration dates listed in the recall notice.
The recall mentions CGMP deviations but does not specify any safety risk or injury mechanism.
The recall notice does not provide a remedy or action step for consumers.
Check for the NDC code 17478-062-35 and expiration dates listed in the recall notice.
We’ve drafted a message you can send Akorn to request your refund or repair — edit it as you like.
Subject: Recall D-0133-2023 — Akorn Akorn Hello, I own a Akorn that is covered by recall D-0133-2023 from Akorn. 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.
