Apotex recalls 0.2%/0.5% eye drops due to potential sterility issues from improper sealing. Affected lots expire Dec 2025. Stop using if you have these specific sizes.
Lack of Assurance of Sterility; atypical weight loss due to improper bottle sealing leading to potential sterility concerns
Apotex is recalling two strengths of eye drops (0.2%/0.5%) that may not be sterile because of sealing problems. This could lead to infections if used improperly. People with prescriptions for these drops should check their lot numbers.
The eye drops may not be sterile because the bottle sealing is faulty. This could lead to infections if the drops are used without proper cleaning or if the bottle is not sealed correctly. The risk is higher for people with weakened immune systems.
Prescription users of Apotex Brimonidine/Timolol eye drops (5mL or 10mL) who received these specific lots. People with diabetes or compromised immune systems are at higher risk for infection.
Check the product label for 'Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution, 0.2%/0.5%'. Look for lot numbers VE0614 (5mL) or VE0616 (10mL) with expiration dates of December 2025.
Look for lot numbers VE0614 (5mL) or VE0616 (10mL) with expiration dates of December 2025.
If you have the recalled lot numbers, discard the eye drops immediately to avoid potential infection.
Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution, 0.2%/0.5% eye drops in 5mL or 10mL sizes.
Check the product label for lot numbers VE0614 (5mL) or VE0616 (10mL) with expiration dates of December 2025.
Yes, if you have the recalled lot numbers, discard them immediately to avoid potential infection.
We’ve drafted a message you can send Apotex to request your refund or repair — edit it as you like.
Subject: Recall D-0676-2025 — Apotex Apotex Hello, I own a Apotex that is covered by recall D-0676-2025 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.
