Akorn recalls 5mL Olopatadine HCL Ophthalmic Solution due to CGMP deviations. This antihistamine eye drop may not meet quality standards. Consumers should contact Akorn for details.
CGMP Deviations:
Akorn is recalling 5mL olopatadine eye drops because of manufacturing quality issues. This could mean the product doesn't meet safety standards, though no specific harm has been reported.
The recall is due to CGMP (Current Good Manufacturing Practices) deviations, which means the product may not meet quality and safety standards. This could lead to the eye drops not working as intended or causing adverse reactions.
People who own or use the recalled olopatadine eye drops are affected. Those with allergies to olopatadine or other ingredients should avoid it.
Check for the product name 'Olopatadine HCL Ophthalmic Solution, USP 0.1%', 5mL bottles, and the lot number 1L03A with expiration date 10/31/2023.
Reach out to Akorn, Inc. for specific instructions on handling the recalled product.
The recall indicates potential quality issues, but no specific safety risks have been reported. Consult Akorn for details.
The official recall does not specify a remedy, so contact Akorn, Inc. for instructions.
Look for the product name 'Olopatadine HCL Ophthalmic Solution, USP 0.1%', 5mL bottles, and lot number 1L03A with expiration date 10/31/2023.
We’ve drafted a message you can send Akorn to request your refund or repair — edit it as you like.
Subject: Recall D-0148-2023 — Akorn Akorn Hello, I own a Akorn that is covered by recall D-0148-2023 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.