Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
LATANOPROST OPHTHALMIC SOLUTION Recalled by Akorn, Inc. Due to Lack of assurance of sterility: product was found...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Akorn, Inc. directly.
Affected Products
LATANOPROST OPHTHALMIC SOLUTION, 0.005%, 125 ug/2.5 mL, packaged in 2.5 mL bottle, Rx only, Manufactured for: Akorn, Inc., Lake Forest, IL 60045, NDC 17478-625-12
Quantity: 107,940 bottles
Why Was This Recalled?
Lack of assurance of sterility: product was found to be empty, under-filled, or leaking.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Akorn, Inc.
Akorn, Inc. has 176 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report