Teva recalls Clear Eyes allergy eye drops due to impurities found in stability testing. Affected lots expire May 2023 through February 2024. No remedy specified in recall notice.
Failed Impurities Specification: Out-of-specification (OOS) stability test result was obtained for unspecified impurity.
Teva Pharmaceuticals is recalling Clear Eyes eye allergy relief drops because stability testing found impurities. This could pose a risk to eye health if the product is used.
The product failed stability testing for an unspecified impurity. This means the eye drops may contain harmful substances that could cause eye irritation or other health issues when used.
People who purchased Clear Eyes eye drops with the specified lot numbers and expiration dates are affected. Those with eye allergies using this product are most at risk.
Check the bottle label for the product name 'Clear Eyes, Once Daily, Eye Allergy Itch Relief' and the lot numbers listed: 114349 (exp. 05/2023), 117396 (exp. 09/2023), 120128 (exp. 11/2023), 114371 (exp. 06/2023), or 123781 (exp. 02/2024).
Look for the lot numbers 114349, 117396, 120128, 114371, or 123781 on the bottle.
The recall states the product failed stability testing for an unspecified impurity, so it may contain harmful substances. Do not use until the manufacturer provides a remedy.
The recall does not specify a remedy, so contact Teva Pharmaceuticals for guidance on what to do with the product.
Check the bottle label for the lot numbers: 114349 (exp. 05/2023), 117396 (exp. 09/2023), 120128 (exp. 11/2023), 114371 (exp. 06/2023), or 123781 (exp. 02/2024).
We’ve drafted a message you can send Teva Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0469-2023 — Teva Pharmaceuticals Teva Pharmaceuticals Hello, I own a Teva Pharmaceuticals that is covered by recall D-0469-2023 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.
