HIGH

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.

Quick Facts at a Glance

Recall Date
March 3, 2026
Hazard Level
HIGH
Brands
Goodsense Eye Drops Original Formula, Good Neighbor Pharmacy Eye Drops Original Formula, Rugby tetrahydrozoline ophthalmic Solution...
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

Hazard Information

Lack of Assurance of Sterility

What You Should Do

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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About This Product

Eye drops with tetrahydrozoline HCl 0.05% are used to relieve eye redness. The products in this recall were widely distributed under multiple store brands and retailers as sterile eye drops.

Why This Is Dangerous

Lack of sterility means the solution may be contaminated. Contaminated eye drops can cause infection, irritation, or injury.

Industry Context

This recall is not presented as part of a broader industry pattern in the materials provided.

Real-World Impact

Users may face eye infections or irritation. The recall covers hundreds of thousands of bottles and spans multiple store brands and distributors.

Practical Guidance

How to identify if yours is affected

  1. Check if you own Goodsense Eye Drops Original Formula or Good Neighbor Pharmacy Eye Drops Original Formula.
  2. Look for NDC 50804-141-01 or UPCs listed in the recall notice.
  3. Check lot numbers RG24E01, RG24G02, RG24G01 and expirations 05/31/26 or 07/31/26.

Where to find product info

Labelling on bottle shows NDC, UPC, and lot number. The recall page provides the official list of identifiers.

What timeline to expect

Refunds or replacements will be processed by the recall program through the distributor network. Specific timelines are not provided.

If the manufacturer is unresponsive

  • Document all contact attempts with the distributor and healthcare provider.
  • File a consumer complaint with the FDA if the company is unresponsive.

How to prevent similar issues

  • Always check recall notices before purchasing OTC eye drops.
  • Buy from reputable retailers and verify packaging integrity.
  • Avoid using eye drops past their expiration date and store per label instructions.

Documentation advice

Keep bottle packaging, purchase receipts, photos of labels including NDC/UPC/lot, and any correspondence with the company.

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. • A

Reported Incidents

No injuries or incidents have been reported.

Key Facts

  • 378,144 bottles recalled nationwide
  • Lack of assurance of sterility
  • NDC 50804-141-01 and multiple UPCs
  • Lot/RG numbers RG24E01, RG24G02, RG24G01
  • Exp 05/31/26 and 07/31/26
  • Distributed by Perrigo Direct and multiple retailers

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

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