Is it safe to keep using the recalled eye drops if the bottle looks fine?

No. The products were recalled for lack of sterility. Stop using them immediately and do not rely on appearance.

How can I tell if my bottle is part of the recall?

Check for the listed lot numbers AR24D01, AR24G01, AR24G02, AR24M01 and the expiration dates 04/30/26, 07/31/26, 10/31/26.

What should I do with recalled product?

Stop using it and contact KC Pharmaceuticals, Inc for guidance on refunds or replacement.

Will I receive a refund or replacement?

Refunds or replacements are handled through KC Pharmaceuticals per recall communications.

Where can I find more information about the recall?

Refer to the FDA enforcement report D-0410-2026 and recall notices from KC Pharmaceuticals.

How long will a refund take?

Timelines vary; recall communications usually provide an estimate, typically several weeks.

What if I already disposed of the product?

Keep any proof of disposal and note the lot and expiration to aid the recall process.

Should I contact my doctor if I used the product?

If you experienced eye irritation or infection, seek medical advice promptly.

Where can I report adverse effects or concerns?

Use official channels in the recall notice and contact your local consumer protection agency as needed.

HIGHMarch 3, 2026

Quality Choice Eye Drops and Foster & Thrive Eye Drops Recalled for Sterility in 303,216 Bottles (24

Quality Choice Moisturizing Relief Eye Drops and Foster & Thrive Advanced Relief Eye Drops are recalled after 303,216 bottles distributed nationwide through Walgreens, CVS and other retailers lack sterility. The defect is lack of assurance of sterility. Consumers should stop using the products immediately and contact KC Pharmaceuticals for guidance.

Quick Facts at a Glance

Recall Date: March 3, 2026
Hazard Level: HIGH
Brands: Quality Choice, Foster & Thrive, GoodSense...
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

These are over-the-counter eye drops marketed to moisturize and relieve redness. They are distributed nationwide through multiple retailers.

Why This Is Dangerous

Lack of sterility raises the risk of eye infection or other contamination-related harm if used." This condition applies to all affected lots.

Industry Context

This recall is not described as part of a broader industry pattern.

Real-World Impact

Consumers may suffer eye infections or irritation. Exposure is limited to those who purchased the recalled lots.

Practical Guidance

How to identify if yours is affected

Identify the product by brand name and lot number AR24D01, AR24G01, AR24G02, AR24M01.
Check expiration dates 04/30/26, 07/31/26, 10/31/26.
Review UPCs and NDCs listed in the recall to confirm identification.

Where to find product info

Look on the product label for UPC and NDC numbers listed in the recall notice.

What timeline to expect

Refunds or replacements are typically processed within 4-6 weeks after recall confirmation.

If the manufacturer is unresponsive

Keep records of all correspondence.
File a complaint with CPSC if the company does not respond within a reasonable time.
Consult a lawyer if injuries occur or the company is unresponsive.

How to prevent similar issues

Buy eye drops from reputable retailers with clear recall policies.
Check labels for sterile-supply assurances and expiration dates before use.
Keep a record of lot numbers and UPCs when storing eye-care products.
Avoid buying from sources without transparent recall information.

Documentation advice

Save the recall notice, purchase receipts, bottle labels showing UPC/NDC, and correspondence with KC Pharmaceuticals for records.

Product Details

Product names: Quality Choice Moisturizing Relief Eye Drops; Foster & Thrive Advanced Relief Eye Drops; Goodsense Eye Drops Advanced Relief Moisturizer; Code Red Eye Drops Redness Relief. Size: 0.5 FL OZ (15 mL) bottles. Quantity recalled: 303,216. Distribution: Nationwide in the United States. Sold at: Walgreens, Kroger, CVS Pharmacy and other retailers. Key identifiers include UPCs and NDCs listed in the recall notice (e.g., UPC 3 11917 20074 3; UPC 0 50428 43544 1; NDCs such as 83324-191-14; 70677-1158-1; 50804-130-01; and other listed codes). Model numbers include AR24D01, AR24G01, AR24G02

Reported Incidents

No injuries or incidents have been reported.

Key Facts

303,216 bottles recalled nationwide
Brands affected include Quality Choice Moisturizing Relief Eye Drops, Foster & Thrive Advanced Relie
Goodsense Eye Drops Advanced Relief Moisturizer, Code Red Eye Drops Redness Relief
Lot numbers AR24D01, AR24G01, AR24G02, AR24M01
Expirations 04/30/26, 07/31/26, 10/31/26
FDA recall D-0410-2026

View Original Recall on FDA - Drug Safety

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Safety Guide

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Safety Assessment

Risk LevelHIGH

Severity Score

8/ 10

Affected Groups

GENERAL

Injury Types

ELECTRICALLACERATIONPOISONINGSUFFOCATIONOTHER

Product Classification

CategoryHealth & Personal Care › Drugs & Medications

Product TypeEye Drops

Product Details

Brands

Quality Choice Foster & Thrive GoodSense Code Red Eye Drops

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Leader Artificial Tears Recalled 589,848 Bottles for Sterility Issue in 2026

Leader Artificial Tears Sterile Lubricant Eye Drops sold nationwide are recalled due to lack of assurance of sterility. The recall involves multiple store-brand lines distributed by Cardinal Health and others. Consumers should stop using the product immediately and follow recall guidance from KC Pharmaceuticals via email.

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