Class III โ€” Low Risk

Low risk โ€” use of or exposure to this product is not likely to cause adverse health consequences.

Lumigan (bimatoprost ophthalmic solution) 0.01% Recalled by Allergan Sales, LLC Due to Failed Impurities/Degradation Specifications.

Date: October 19, 2017
Company: Allergan Sales, LLC
Status: Terminated
Source: FDA (Drug)

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 Allergan Sales, LLC directly.

Affected Products

Lumigan (bimatoprost ophthalmic solution) 0.01%, 2.5 mL bottle, Rx only, Allergan, Irvine, CA 92612. NDC# 0023-3205-03

Quantity: 153,616 bottles

Why Was This Recalled?

Failed Impurities/Degradation Specifications.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Allergan Sales, LLC

Allergan Sales, LLC has 14 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report