K.C. Pharmaceuticals recalls sterile 0.5 fl oz eye drops due to lack of assurance of sterility. Consumers should check product labels for NDC 70000-0457-1 or similar codes to determine if affected.
Lack of Assurance of Sterility
K.C. Pharmaceuticals is recalling sterile lubricating eye drops that may not be sterile. This could lead to infections if used without proper sterility.
The eye drops lack assurance of sterility, meaning they might contain harmful bacteria or contaminants. Using non-sterile eye drops can cause infections, especially in individuals with sensitive eyes or existing eye conditions.
People who own or use the recalled eye drops, especially those with eye conditions requiring frequent lubrication. Those with compromised immune systems may be at higher risk.
Check for the product name 'Ultra Lubricating Eye Drops' with NDC 70000-0457-1 or similar codes. Look for lot numbers SU24E01, SU24E02, or SU24K01 with expiration dates up to 9/30/26.
Look for the NDC code 70000-0457-1 or similar codes on the bottle to confirm if it's part of the recall.
If you have the recalled eye drops, discard them immediately to avoid potential infection risks.
The recall is due to a lack of assurance of sterility, which means the eye drops might not be sterile and could cause infections.
Check the product label for NDC 70000-0457-1 or similar codes, and lot numbers SU24E01, SU24E02, or SU24K01 with expiration dates up to 9/30/26.
If you have used the recalled eye drops, contact your doctor or healthcare provider to discuss potential infection risks.
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-0412-2026 — K.C. Pharmaceuticals K.C. Pharmaceuticals Hello, I own a K.C. Pharmaceuticals that is covered by recall D-0412-2026 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.
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