Apotex recalls 5mL prescription eye drops (0.2%/0.5%) due to lack of sterility assurance. This could cause infections if used improperly. Check NDC 60505-0589-1 and lots VJ8599 or VL1668.
Lack of Assurance of Sterility
Apotex is recalling prescription eye drops that may not be sterile, which could lead to eye infections. This is a serious risk for people using the medication as directed.
The eye drops may not be sterile, meaning they could introduce harmful bacteria into the eye. This can cause infections that might lead to vision problems or other complications.
People with a prescription for these eye drops are affected. Those using the medication without proper sterility checks are at highest risk.
Check the product label for 'Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution 0.2%/0.5%', 5 mL, Rx Only. Look for NDC 60505-0589-1 and lots VJ8599 or VL1668.
Immediately stop using the recalled eye drops as they may not be sterile and could cause infections.
No, the product may not be sterile and could cause infections. Do not use it.
The NDC number is 60505-0589-1.
Check the product label for NDC 60505-0589-1 and lots VJ8599 or VL1668.
We’ve drafted a message you can send Apotex to request your refund or repair — edit it as you like.
Subject: Recall D-0407-2026 — Apotex Apotex Hello, I own a Apotex that is covered by recall D-0407-2026 from Apotex. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
