KC Pharmaceuticals recalled 182,424 Sterile Eye Drops AC bottles sold nationwide under multiple brands including Quality Choice Eye Drops Irritation Relief and Goodsense Ultra Lubricant Eye Drops. The recall cites a lack of assurance of sterility. Consumers should stop using the product immediately and contact KC Pharmaceuticals for guidance.
Lack of Assurance of Sterility
Consumers and healthcare providers should stop using this product immediately. Contact K.C. Pharmaceuticals, Inc or your healthcare provider for guidance. Notification method: E-Mail
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Sterile Eye Drops AC are ophthalmic solutions used to soothe irritation and redness. The products in this recall are sold under multiple brand names across various retailers. They appear as 0.5 fl oz bottles and were distributed nationwide in the US.
A lack of sterility assurance means the product could be contaminated. Contaminated eye drops can cause infections or other serious eye injuries requiring medical treatment.
This recall is not indicated as part of a broader industry pattern.
Consumers across the US could be exposed to contaminated eye drops. The recall affects 182,424 bottles, urging immediate cessation of use and guidance from the manufacturer for refunds or replacements.
Recall details available on FDA enforcement site and enforcement report D-0409-2026; packaging and UPC/NDC codes referenced in recall notice
Refunds or replacements typically take 4-8 weeks after confirmation of eligibility
Keep the product packaging, batch number, purchase receipt, and all recall correspondence for records
Product: Sterile Eye Drops AC Size: 0.5 fl oz (15 mL) Lot numbers: AC24E01 Expiration: 05/31/2026 Distributors/brands (examples): Quality Choice Eye Drops Irritation Relief; Goodsense Ultra Lubricant Eye Drops; Meijer Seasonal Itching and Redness Relief; Meijer Distribution, Inc.; Walgreens Eye Drops; H-E-B A.C. Eye Drops; Discount Drug Mart Eye Drops; Perrigo Direct Goodsense lines; TopCare Health; Equaline; Best Choice Quantity recalled: 182,424 bottles Distribution: Nationwide in the United States UPC/NDC references cited in recall: UPC 0 70038 47010 6; NDC 83324-190-14; UPC 0 93351 01158 0
No injuries or incidents have been reported.
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