K.C. Pharmaceuticals recalls 0.5 fl oz dry eye relief eye drops due to lack of assurance of sterility. Consumers should check product labels for NDC 57896-181-05 or similar identifiers.
Lack of Assurance of Sterility
K.C. Pharmaceuticals is recalling dry eye relief eye drops that may not be sterile. This could lead to infections if used improperly. The recall affects specific batches sold through various pharmacies and drugstores.
The eye drops lack assurance of sterility, meaning they might contain harmful bacteria. Using non-sterile eye drops can cause infections, especially in people with dry eyes who rely on them for relief.
People who purchased the recalled dry eye relief eye drops from pharmacies or drugstores listed in the recall. Those with dry eye conditions or using the product regularly are at higher risk.
Check for the product name 'Dry Eye Relief Eye Drops' with NDC numbers like 57896-181-05, 11822-1067-2, or 70000-0502-1. Look for lot numbers LT24E01 through LT24G01 with expiration dates up to May 31, 2026.
Look for NDC numbers such as 57896-181-05 or 11822-1067-2 on the bottle.
Ask your pharmacist if you have the recalled eye drops and whether they can provide a replacement.
The recall is due to a lack of assurance of sterility, which could lead to infections if the eye drops are not properly sterile.
Check for NDC numbers like 57896-181-05 or lot numbers LT24E01 through LT24G01 with expiration dates up to May 31, 2026.
Contact your pharmacist to check if you have the recalled product and ask about a replacement or return.
We’ve drafted a message you can send K.C. Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0411-2026 — K.C. Pharmaceuticals K.C. Pharmaceuticals Hello, I own a K.C. Pharmaceuticals that is covered by recall D-0411-2026 from K.C. Pharmaceuticals. 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.
