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Stop using now Drug recall · FDA · Published July 29, 2026

Clear Eyes Eye Drops Recalled for Sterility Risk

Prestige Brands recalls Clear Eyes Maximum Itchy Eye Relief drops due to lack of sterility assurance. Check your lot number and expiration date.

🇺🇸 FDA recall #D-0766-2026DrugClear Eyes ›
✎ GovInfoNow plain-language explainer

What happened, in plain English

Prestige Brands Holdings is recalling one lot of CLEAR EYES Maximum Itchy Eye Relief because there is no assurance that the product remains sterile. The recall covers approximately 39,060 bottles distributed nationwide in the USA. Using non-sterile eye drops can introduce bacteria or other contaminants to the eye. Read more at govinfonow.com/recall/454412-clear-eyes-eye-drops-recalled-for-sterility-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/454412-clear-eyes-eye-drops-recalled-for-sterility-risk · Updated October 9, 2026 · FDA enforcement record: FDA #D-0766-2026

Cite this page

“Clear Eyes Eye Drops Recalled for Sterility Risk.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/454412-clear-eyes-eye-drops-recalled-for-sterility-risk. Based on FDA recall #D-0766-2026 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0766-2026%22&limit=1).

Why it’s dangerous

The product was labeled as sterile, but manufacturing or quality control issues mean sterility cannot be assured. This lack of assurance creates a risk that the eye drops may be contaminated with microorganisms, which can cause serious eye infections when applied to sensitive tissue.

Who’s affected

Consumers across the United States who purchased CLEAR EYES Maximum Itchy Eye Relief, specifically those with the affected lot number and expiration date. Individuals using these drops for itchy eyes are at risk of potential infection from contamination.

How to tell if you have this one

Check your bottle for NDC: 67172-999-01 and UPC: 6 78112 65920 3. Specifically look for Lot number 2552A with an expiration date of 09/30/2027. The product is a 0.5 fl oz (15 mL) dropper bottle distributed by Medtech Products Inc.

  • Brand
    Clear Eyes
  • Product
    CLEAR EYES Maximum Itchy Eye Relief, 0.5 fl oz (15 mL) per dropper bottle, Sterile, Dist. by Medtech Products Inc
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Stop using the eye drops

    Do not use the recalled CLEAR EYES Maximum Itchy Eye Relief drops if you have the specific lot number and expiration date listed in the record.

  2. Dispose of or return the product

    The recall record does not specify a remedy such as a refund or replacement, so consumers should handle the product safely according to local guidelines for unused medications.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide in the USA.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 21 days after the firm started it.

1. Firm started the recall: Jul 29, 202612. FDA classified it Class II: Aug 14, 202623. Published in FDA’s Enforcement Report: Aug 19, 202634. Added to GovInfoNow: Aug 27, 202642026
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. Added to GovInfoNow

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #D-0766-2026 (July 29, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0766-2026 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 9, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA