Apotex recalls Brimonidine Tartrate Ophthalmic Solution 0.15% (Rx only) due to cap cracks that may compromise sterility. Affected units have specific NDC/UPC codes and expiration dates. Consumers should contact Apotex for details.
Lack of sterility assurance: Cracks have developed in some of the units caps of Brimonidine tartrate ophthalmic solution bottles. There is a possibility the broken cap may impact sterility.
Apotex is recalling Brimonidine Tartrate Ophthalmic Solution 0.15% (Rx only) because some bottles have cracks in the cap that could allow contamination. This poses a risk of infection if the medication is not sterile.
Cracks in the bottle caps may allow contaminants to enter the solution, potentially causing eye infections. The medication is for prescription use only and requires sterility to be safe.
People with prescriptions for Brimonidine Tartrate Ophthalmic Solution 0.15% who own the recalled bottles. Those with eye conditions requiring this medication are most at risk.
Check for bottles labeled 'Brimonidine Tartrate Ophthalmic Solution 0.15%, Rx Only' with specific NDC numbers: 60505-0564-1 (5mL), 60505-0564-2 (10mL), or 60505-0564-3 (15mL). The expiration dates for these units range from February 2024 to April 2024.
Identify the NDC code on the bottle (60505-0564-1, 60505-0564-2, or 60505-0564-3) and expiration date.
Reach out to Apotex for instructions on how to return or replace the recalled product.
The product is not safe to use as recalled units have cracks in the cap that could compromise sterility. Do not use these bottles.
Check for the NDC codes 60505-0564-1 (5mL), 60505-0564-2 (10mL), or 60505-0564-3 (15mL) and expiration dates between February 2024 and April 2024.
Contact Apotex for instructions on returning or replacing the product.
We’ve drafted a message you can send Apotex to request your refund or repair — edit it as you like.
Subject: Recall D-0433-2023 — Apotex Apotex Hello, I own a Apotex that is covered by recall D-0433-2023 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
