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
- Source
- FDA
- Category
- Drugs & Medications
- Recall ID
- fda-D-0407-2026
- Classification
- Class II
- Recalled
- March 5, 2026
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