Allergan Sales, LLC recalls Combigan (brimonidine tartrate/timolol maleate ophthalmic solution) 0.2%/0.5%, Rx only, packaged in a) 2.5 mL NDC# 0023…

Recall date

October 19, 2017

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D-0077-2018

FDA classification

Class III

Brand / firm

Allergan Sales, LLC

Sold / distributed

Nationwide and Barbados, Curacao, Dominican Republic, Guyana, Jamaica, and Trinidad and Tobago.

Why it was recalled

Failed Impurities/Degradation Specifications.

Class III means the product violates regulations but is not likely to cause harm.

What was recalled

Combigan (brimonidine tartrate/timolol maleate ophthalmic solution) 0.2%/0.5%, Rx only, packaged in a) 2.5 mL NDC# 0023-9211-03; b) 5 mL (NDC# 0023-9211-05); c) 10 mL (NDC# 0023-9211-10); d) 15 mL (NDC# 0023-9211-15) bottles, Manufactured By: Allergan, Irvine, CA 92612..