BRS Analytical Services recalls specific lots of artificial tears eye lubricant drops due to cGMP deviations and lack of sterility assurance. Consumers should check product labels for affected lots and contact the manufacturer for guidance.
cGMP deviations and lack of assurance of sterility.
BRS Analytical Services has recalled certain lots of artificial tears eye lubricant drops because of cGMP deviations and lack of sterility assurance. This could lead to infections if the product is used without proper sterility.
The product was made with cGMP deviations and lacks proper sterility assurance, which could lead to infections if the drops are used. This is a serious concern for eye health.
People who own or use the recalled eye lubricant drops are affected. Those with eye conditions requiring frequent lubrication are at higher risk.
Check the product label for the lot numbers listed: 126-129, 162-169, 193-199. The expiration dates range from October 2025 to October 2026.
Look for the lot numbers 126-129, 162-169, or 193-199 on the bottle.
The product was made with cGMP deviations and lacks proper sterility assurance, which could lead to infections if used.
Check the product label for the lot numbers listed and contact BRS Analytical Services for further guidance.
Yes, the product could cause infections due to lack of sterility assurance, so it is recommended to stop using it if you have the recalled lot numbers.
We’ve drafted a message you can send BRS Analytical Services to request your refund or repair — edit it as you like.
Subject: Recall D-0404-2025 — BRS Analytical Services BRS Analytical Services Hello, I own a BRS Analytical Services that is covered by recall D-0404-2025 from BRS Analytical Services. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.