Rohto recalls cooling eye drops due to potential lack of sterility. Affected lots from Vietnam with specific expiration dates. Consumers should check labels and contact the manufacturer for details.
Lack of Assurance of Sterility
Rohto is recalling its cooling eye drops because they may not be sterile. This could lead to infections if used improperly. The recall affects specific batches sold in the U.S. with certain expiration dates.
The eye drops may not be sterile, which could cause infections if used. This is a risk for people who use the product without proper hygiene or have compromised immune systems.
People who own or use Rohto Cooling Eye Drops Dry Aid (povidone 0.68%, propylene glycol 0.3%) with the listed lot numbers and expiration dates are affected. Those with sensitive eyes or recent eye injuries are at slightly higher risk.
Check the label for the lot numbers: 4G1VA (exp. 2027/06), 4J1VA (exp. 2027/09), 5A1V (exp. 2027/12), 5D1VA (exp. 2028/03), 5G1VA (exp. 2028/06), 512V (exp. 2028/08), and 5L2VA (exp. 2028/11). The product is sold in the U.S. with specific expiration dates.
Look for the lot numbers and expiration dates listed above to confirm if your product is affected.
The recall states there is a lack of assurance of sterility, which could lead to infections. Do not use the affected lots until the manufacturer provides further instructions.
Check the label for the lot numbers: 4G1VA (exp. 2027/06), 4J1VA (exp. 2027/09), 5A1V (exp. 2027/12), 5D1VA (exp. 2028/03), 5G1VA (exp. 2028/06), 512V (exp. 2028/08), and 5L2VA (exp. 2028/11).
The recall does not specify a remedy, so contact Rohto directly for further instructions on disposal or replacement.
We’ve drafted a message you can send Rohto to request your refund or repair — edit it as you like.
Subject: Recall D-0720-2026 — Rohto Rohto Hello, I own a Rohto that is covered by recall D-0720-2026 from Rohto. 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.
