BRS Analytical Services recalls sterile lubricant eye drops (0.5 fl oz) due to cGMP deviations and lack of sterility assurance. Affected lots from 10/02/25 to 7/31/26.
cGMP deviations and lack of assurance of sterility.
BRS Analytical Services has recalled sterile lubricant eye drops that may not be sterile due to manufacturing quality issues. Using these drops could lead to eye infections or other serious complications if the product is contaminated.
The eye drops were produced without proper quality control, meaning they might not be sterile. If contaminated, they could cause serious eye infections, especially in people with weakened immune systems or sensitive eyes.
People who purchased the recalled eye drops from the listed lots between October 2025 and July 2026 are affected. Those with sensitive eyes or compromised immune systems are at higher risk of infection.
Check the bottle label for the product name 'Polyvinyl Alcohol Ophthalmic Solution 1.4%'. Look for the lot numbers listed: 120 through 179, with expiration dates from October 2025 to July 2026.
Look for the lot numbers 120 through 179 on the bottle with expiration dates from October 2025 to July 2026.
Reach out to BRS Analytical Services for further assistance or to confirm if your product is affected.
The recall indicates potential contamination risks, so it's best to stop using them until you confirm they are safe.
Check the bottle for lot numbers 120 through 179 with expiration dates from October 2025 to July 2026.
Contact BRS Analytical Services to confirm if your product is affected and get guidance on next steps.
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-0408-2025 — BRS Analytical Services BRS Analytical Services Hello, I own a BRS Analytical Services that is covered by recall D-0408-2025 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.
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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.
