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Serious recall: Injury is possible or has been reported. Take action promptly.

Apotex Corp. 2026-03-25 Health serious FDA
Health · FDA · Recall #FDA-D-0407-2026

Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution 0.2%/0.5%*, 5 mL, Rx Only,… Recall

Issued March 25, 2026 · Apotex Corp.

In March 2026, Apotex Corp. recalled the Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution 0.2%/0.5%*, 5 mL, Rx Only,…, a serious health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

Lack of Assurance of Sterility

What you should do

  1. 1 Stop using Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution 0.2%/0.5%*, 5 mL, Rx Only,… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Apotex Corp. to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Apotex Corp.
Category
Health
Recall date
March 25, 2026
Units affected
Not reported
Sold at
U.S. Nationwide
Recall number
FDA-D-0407-2026
Made in
United States
Issuing agency
FDA

In context

  • Apotex Corp. has 9 recalls in our database.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 356th Health recall we've logged in 2026.
Read the official FDA notice

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