Teva Pharmaceuticals recalls Brinzolamide Ophthalmic Suspension 1% dropper bottles due to a cap notch that may break off and block the dropper, preventing product dispensing.
Defective Container: The notch in the cap that fits into the nozzle of the dropper could break off and block the dropper possibly resulting in the product not dispensing.
Teva Pharmaceuticals is recalling Brinzolamide Ophthalmic Suspension 1% dropper bottles because the cap's notch could break off and block the dropper, potentially preventing the medication from dispensing. This could lead to incomplete treatment if the medication isn't properly administered.
The cap notch that fits into the dropper nozzle may break off, blocking the dropper and preventing the medication from dispensing. This could lead to incomplete treatment if the medication isn't properly administered.
People who have the recalled Brinzolamide Ophthalmic Suspension 1% dropper bottles (10 ml or 15 ml) from Teva Pharmaceuticals. Those with eye conditions requiring this medication are most at risk.
Check for Brinzolamide Ophthalmic Suspension 1% dropper bottles with NDC 0591-2127-79 (10 ml) or NDC 0591-2127-12 (15 ml). The product was manufactured in India by Indoco Remedies Limited and distributed by Teva Pharmaceuticals USA.
Look for NDC codes 0591-2127-79 (10 ml) or 0591-2127-12 (15 ml) on the bottle.
The recall is for potential blockage of the dropper, but the product is generally safe if the cap notch does not break off.
Check for NDC codes 0591-2127-79 (10 ml) or 0591-2127-12 (15 ml) on the bottle.
The recall does not specify a remedy, so contact Teva Pharmaceuticals for guidance.
We’ve drafted a message you can send Teva Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0373-2022 — Teva Pharmaceuticals Teva Pharmaceuticals Hello, I own a Teva Pharmaceuticals that is covered by recall D-0373-2022 from Teva Pharmaceuticals. 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.
