Apotex Corp. recalls Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution 0.2%/0.5%*
- Recalling company
- Apotex Corp.
- Product
- Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution 0.2%/0.5%*, 5 mL, Rx Only, Sterile, Apotex Corp. Manufactured for: Apotex Corp., Weston, FL 33326, NDC 60505-0589-1.
- Reason
- Lack of Assurance of Sterility
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Mar 5, 2026
- Reported
- Mar 25, 2026
- Distribution
- U.S. Nationwide
- Status
- Ongoing
- Quantity
- 107,136 vials
- Lot / codes
- Lots VJ8599, Exp Date 09/30/2026 & VL1668, Exp Date 01/31/2027
- Company location
- Weston, FL
- Recall type
- Voluntary: Firm initiated
- Recall number
- D-0407-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number D-0407-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.