BRS Analytical Services recalls Carboxymethylcellulose Sodium Eye Lubricant (0.5%) due to cGMP deviations and lack of sterility assurance. Affected lots from 2023-2027.
cGMP deviations and lack of assurance of sterility.
BRS Analytical Services has recalled a specific eye lubricant product due to manufacturing issues that could compromise sterility. This means the product might not be safe for eye use, especially if it's been stored for a long time.
The product was made under conditions that didn't meet strict quality standards, which could mean it's not sterile. Using non-sterile eye drops might cause infections or irritation, especially for people with sensitive eyes.
People who have purchased the recalled eye lubricant from the listed lots. Those with sensitive eyes or who use the product frequently are at slightly higher risk.
Check the bottle label for the product name 'Carboxymethylcellulose Sodium Ophthalmic Solution 0.5%'. Look for the lot numbers listed in the recall (e.g., Lot 103 through Lot 224) and expiration dates from April 2025 through March 2027.
Look for the product name and lot numbers listed in the recall to confirm if your bottle is affected.
If your bottle has a lot number from the list (e.g., Lot 103 to Lot 224), dispose of it safely to avoid potential eye infections.
The product may not be sterile due to manufacturing issues, so it's recommended to discard affected lots to avoid potential eye infections.
Check the bottle label for the product name and lot numbers listed in the recall (e.g., Lot 103 through Lot 224).
Discard the product safely to avoid potential eye infections, as the product may not be sterile.
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-0406-2025 — BRS Analytical Services BRS Analytical Services Hello, I own a BRS Analytical Services that is covered by recall D-0406-2025 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.
