K.C. Pharmaceuticals recalls sterile eye drops for redness relief that may not be sterile, posing a risk of infection. Consumers should check product details and contact the manufacturer for guidance.
Lack of Assurance of Sterility
K.C. Pharmaceuticals is recalling sterile eye drops for redness relief due to a lack of assurance of sterility. This could lead to eye infections if the product is not properly sterile. Consumers should stop using the product and contact the manufacturer for more information.
The eye drops may not be sterile, which can lead to infections in the eye. This is a serious risk because the product is intended for direct use on the eye and can cause infections if not properly sterile.
People who own or use the recalled sterile eye drops for redness relief are affected. Those with compromised immune systems or existing eye conditions are at higher risk of infection.
Check for the product name 'Sterile EYE DROPS REDNESS LUBRICANT' with the following lot numbers: RL24D01 (expiring 04/30/26) or RL24F01/RL24F02 (expiring 06/30/26). The product is sold under various brand names through pharmacies and drugstores.
Immediately stop using the recalled eye drops as they may not be sterile and could cause eye infections.
Sterile EYE DROPS REDNESS LUBRICANT (glycerin 0.25% and naphazoline HCl 0.012%), 0.5 fl oz (15 mL) bottles with lot numbers RL24D01 or RL24F01/RL24F02.
Check the product label for the lot numbers RL24D01 (expiring 04/30/26) or RL24F01/RL24F02 (expiring 06/30/26). The product is sold under various brand names through pharmacies and drugstores.
Immediately stop using the product and contact K.C. Pharmaceuticals for further instructions.
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-0414-2026 — K.C. Pharmaceuticals K.C. Pharmaceuticals Hello, I own a K.C. Pharmaceuticals that is covered by recall D-0414-2026 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.
