Scope Health recalls Optase Dry Eye Intense Drops (Glycerin 0.2%) due to lack of sterility assurance. Products with specific lot numbers and expiration dates are affected. Consumers should check their product details and contact Scope Health for guidance.
Lack of Assurance of Sterility
Scope Health is recalling Optase Dry Eye Intense Drops (Glycerin 0.2%) because they may not be sterile. This could lead to infections if used improperly. The recall affects specific lot numbers and expiration dates.
The product may not be sterile, which could lead to infections if used. This lack of sterility assurance is a serious concern for eye drops that are meant to be used directly on the eye.
People who own or use the recalled Optase Dry Eye Intense Drops are affected. Those with the specific lot numbers and expiration dates listed are most at risk.
Check the product label for the lot numbers: 8T98, 9T31, 9T32, 2V13, 2V14, 2V15, 3V35, 3V36, 3V37, 5V45, 5V46, 9V12, 1X57, 1X70, 1X84. Also look for the expiration dates listed: 30/04/26, 30/06/26, 31/08/26, 30/09/26, 31/03/27, 31/05/27.
Look for the lot numbers and expiration dates on the product label to confirm if it is recalled.
Optase Dry Eye Intense Drops (Glycerin 0.2%) packaged in 0.33 fl oz, sterile, with specific lot numbers and expiration dates.
Check the product label for lot numbers: 8T98, 9T31, 9T32, 2V13, 2V14, 2V15, 3V35, 3V36, 3V37, 5V45, 5V46, 9V12, 1X57, 1X70, 1X84 and expiration dates: 30/04/26, 30/06/26, 31/08/26, 30/09/26, 31/03/27, 31/05/27.
The recall record does not specify a remedy, so contact Scope Health directly for guidance.
We’ve drafted a message you can send Scope Health to request your refund or repair — edit it as you like.
Subject: Recall D-0499-2026 — Scope Health Scope Health Hello, I own a Scope Health that is covered by recall D-0499-2026 from Scope Health. 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.
