Goodsense Eye Drops Original Formula Recall 378,144 Bottles Nationwide 2026
Goodsense Eye Drops Original Formula, distributed nationwide, has recalled 378,144 sterile bottles in 2026 due to lack of assurance of sterility. The sterile ophthalmic solution may be contaminated. Consumers and healthcare providers should stop using immediately and contact K.C. Pharmaceuticals for refunds or replacements.
Product Details
• NDC: 50804-141-01 (Perrigo Direct).
• UPCs: 3 11917 20073 6; 3 11917 20076 7; 0 1110 38597 0; 0 72036 71302 5; 0 41220 43747 4; 7 61606 16500 3; 1 94283 65185 8; 0 95072 00556 5; 24385-075-05; 0 36800 03639 0; 0 70038 47011 3.
• Models/Lots: RG24E01; RG24G02; RG24G01 with Exp 05/31/26 and 07/31/26.
• Product type: Original Formulation Sterile Eye Drops (Tetrahydrozoline HCl 0.05%).
• Manufactured for: Lil' Drug Store Products, Inc. (Cedar Rapids, IA).
• Distributed nationwide by Perrigo Direct, Walgreens Co., The Kroger Co., Circle K, H-E-B, Harris Teeter, Discount Drug Mart, and others.
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The Hazard
The product lacks assurance of sterility. Use of non-sterile eye drops could cause eye infections or other ocular complications. The recall covers products sold nationwide in the United States.
Reported Incidents
No injuries or incidents have been reported.
What to Do
1. Stop using the product. 2. Consult a healthcare provider if you have used these eye drops and experience eye irritation, redness, or discharge. 3. Contact K.C. Pharmaceuticals, Inc for guidance on refunds or replacements, or follow the FDA recall notice for instructions. 4. Check the FDA recall page for updates on refunds and disposal guidance.
Contact Information
FDA recall notice: https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=D-0413-2026. Specific refund contact available through K.C. Pharmaceuticals, Inc via recall notice.