HIGHFDA DRUG

KC Pharmaceuticals Recalled Sterile Eye Drops AC 182,424 Bottles Nationwide (2026)

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.

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 Eye Drops Irritation Relief, Goodsense Ultra Lubricant Eye Drops, Meijer Seasonal Itching and Redness Relief...
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 Eye Drops Irritation Relief, Goodsense Ultra Lubricant Eye Drops, Meijer Seasonal Itching and Redness Relief, Quality Choice +2 more
Product type
Sterile Eye Drops
Model numbers
AC24E01
UPC codes
83324-190, 50804-160, 41250-598, 83324-190-14, 50804-160-01, 41250-598-01
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

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.

Why This Is Dangerous

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.

Industry Context

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

Real-World Impact

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.

Practical Guidance

How to identify if yours is affected

  1. Check bottle for Lot AC24E01
  2. Check expiration date 05/31/26
  3. Note the brands include Quality Choice Eye Drops Irritation Relief, Goodsense Ultra Lubricant Eye Drops, Meijer Seasonal Itching and Redness Relief
  4. If affected, stop using and set aside for disposal or return
  5. Contact KC Pharmaceuticals for guidance via the recall email

Where to find product info

Recall details available on FDA enforcement site and enforcement report D-0409-2026; packaging and UPC/NDC codes referenced in recall notice

What timeline to expect

Refunds or replacements typically take 4-8 weeks after confirmation of eligibility

If the manufacturer is unresponsive

  • Document all communications with KC Pharmaceuticals
  • Escalate to FDA CPSC if no response within 2-4 weeks
  • Consider legal consultation for unresolved refunds

How to prevent similar issues

  • Always check sterility assurances for ophthalmic products
  • Verify lot numbers and expiration dates before use
  • Be wary of multiple store-brand lines sharing the same active ingredients
  • Keep records of purchase and recall notices

Documentation advice

Keep the product packaging, batch number, purchase receipt, and all recall correspondence for records

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Product Details

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

Reported Incidents

No injuries or incidents have been reported.

Key Facts

  • Lot AC24E01 with Exp. 05/31/26
  • Distributed under multiple store brands (Quality Choice, Goodsense, Meijer, Walgreens, H-E-B, etc.)
  • Reason: Lack of Assurance of Sterility
  • Stop use immediately and seek guidance from KC Pharmaceuticals

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

Product Details

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