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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.

Official notice

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DRUG
Recall date
March 3, 2026
Status
ACTIVE
Severity
8/10

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

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
Quality Choice, Foster & Thrive, GoodSense, Code Red Eye Drops
Product type
Eye Drops
Model numbers
AR24D01, AR24G01, AR24G02, AR24M01
UPC codes
83324-191, 70677-1158, 50804-130, 83817-963, 83324-191-14, 70677-1158-1, 50804-130-01, 83817-963-01
Sizes
0.5 FL OZ (15 mL)
Sold at
Multiple Retailers
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    March 3, 2026

  2. Reported by FDA DRUG

    April 8, 2026

  3. RecallRadar source check

    April 15, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

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

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

  1. Identify the product by brand name and lot number AR24D01, AR24G01, AR24G02, AR24M01.
  2. 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.

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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
  • FDA recall D-0410-2026

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
ELECTRICALLACERATIONPOISONINGSUFFOCATIONOTHER

Product Details

Model Numbers
AR24D01
AR24G01
AR24G02
AR24M01
UPC Codes
83324-191
70677-1158
50804-130
+5 more
Affected States
ALL
Report Date
April 8, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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