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High risk Drugs & MedicationsClass II

Apotex Brimonidine/Timolol Eye Drop Recall

Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution 0.2%/0.5%*, 5 mL, Rx Only, Sterile, Apotex Corp. Manufactured for: Apotex Corp., We

Updated March 5, 2026

Apotex Corp. is recalling Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution because sterility cannot be assured. Use of a non-sterile eye drop can cause serious infection.

Is the Apotex Corp. recalled? Yes. This product was recalled by FDA on March 5, 2026. Details below.

What is recalled

Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution 0.2%/0.5%, 5 mL, Rx Only, Sterile, manufactured by Apotex Corp., Weston, FL 33326. NDC: 60505-0589-1.

Am I affected

You're affected if you have a prescription bottle of this eye drop with NDC 60505-0589-1 on the label and it was manufactured by Apotex Corp.

What to do right now

Stop using this eye drop immediately. Contact your pharmacy or the manufacturer Apotex Corp. to return the product and get a replacement or refund. Do not use any remaining solution.

The hazard

Lack of Assurance of Sterility

Brands affected

Apotex Corp.
Source
FDA
Category
Drugs & Medications
Recall ID
fda-D-0407-2026
Classification
Class II
Recalled
March 5, 2026
Read the official notice

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