K.C. Pharmaceuticals recalls 0.5 fl oz dry eye relief eye drops with CGMP deviations in fill line documentation. Consumers should check product labels for lot numbers and expiration dates.
CGMP Deviations: good manufacturing deficiencies related to a lack of documentation of the fill line.
K.C. Pharmaceuticals is recalling dry eye relief eye drops due to manufacturing issues that lack proper documentation of the fill line. This could lead to inconsistent product quality but does not pose an immediate safety risk.
The recall is due to good manufacturing practice (CGMP) deviations where the fill line documentation was not properly maintained. This could result in inconsistent product quality but does not involve immediate safety hazards like injury or illness.
People who purchased the dry eye relief eye drops from Walmart, DG Health, Sunmark, TopCare Health, HealthMart, Military Exchanges, Meijer, H.E.B, or GeriCare stores. Those most at risk are individuals using the product for dry eye relief.
Check the product label for the lot numbers LT21FO2 or LT21F03 with an expiration date of June 2023. The product comes in 0.5 fl oz (15mL) bottles with specific UPC and NDC codes listed in the recall notice.
Look for lot numbers LT21FO2 or LT21F03 with an expiration date of June 2023 on the bottle.
No, the recall is for manufacturing documentation issues, not an immediate safety hazard. The product is safe to use but should be checked for the specific lot numbers.
The product was sold at Walmart, DG Health, Sunmark, TopCare Health, HealthMart, Military Exchanges, Meijer, H.E.B, and GeriCare stores.
Check the product label for lot numbers LT21FO2 or LT21F03 with an expiration date of June 2023.
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-0898-2023 — K.C. Pharmaceuticals K.C. Pharmaceuticals Hello, I own a K.C. Pharmaceuticals that is covered by recall D-0898-2023 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.
