Clear Eyes Eye Drops Recall: FDA Contamination Alert
Prestige Consumer Healthcare is recalling nearly 40,000 bottles of Clear Eyes Maximum Itchy Eye Relief eye drops because of potential contamination and concerns about sterility. The nationwide recall involves 15mL bottles with lot code 2552A and an expiration date of September 30, 2027.
A New York-based consumer healthcare company is recalling nearly 40,000 bottles of Clear Eyes eye drops over concerns about the product's sterility.
Prestige Consumer Healthcare initiated the recall on July 29, 2026, due to a “lack of assurance of sterility,” according to a U.S. Food and Drug Administration notice.
The FDA notice states that the recall is due to potential contamination.
Which Clear Eyes Eye Drops Are Recalled?
The recall affects 15mL bottles of Clear Eyes Maximum Itchy Eye Relief.
According to the product description provided in the recall information, the eye drops are intended to help mitigate:
- Itchiness
- Redness
- Other eye irritations
The affected eye drops were distributed nationwide.
FDA Recall Classification
The FDA categorized the Clear Eyes eye drops recall as Class II.
According to the FDA definition provided in the supplied information, a Class II recall involves a product that could cause temporary or medically reversible adverse health consequences.
Clear Eyes Recall Information
| Recall Detail | Information |
|---|---|
| Company | Prestige Consumer Healthcare |
| Product | Clear Eyes Maximum Itchy Eye Relief |
| Bottle Size | 15mL |
| Recall Date | July 29, 2026 |
| Recall Reason | Potential contamination / lack of assurance of sterility |
| Distribution | Nationwide |
| FDA Recall Classification | Class II |
| Recall Number | D-0766-2026 |
| Lot Code | 2552A |
| Expiration Date | September 30, 2027 |
Recall Number: D-0766-2026
The FDA recall information supplied for this Clear Eyes product lists:
- Recall number: D-0766-2026
- Lot code: 2552A
- Expiration date: September 30, 2027
Consumers can use these details to identify whether their Clear Eyes product matches the recalled information provided in the notice.
Why Was Clear Eyes Maximum Itchy Eye Relief Recalled?
The recall was initiated because of a lack of assurance of sterility and concerns about potential contamination, according to the supplied FDA notice information.
The FDA classified the recall as Class II, meaning the recalled product could potentially cause temporary or medically reversible adverse health consequences.
Company Response
Prestige Consumer Healthcare did not immediately respond to a request for comment, according to the supplied information.
What Consumers Should Check
Consumers who have Clear Eyes Maximum Itchy Eye Relief should compare the product information with the recalled details:
- Product: Clear Eyes Maximum Itchy Eye Relief
- Size: 15mL
- Lot code: 2552A
- Expiration date: September 30, 2027
- Recall number: D-0766-2026
If the product information matches the supplied recall details, consumers should refer to the official FDA recall notice for the latest instructions.
Important: This article is based only on the supplied recall information. Specific instructions about returning, disposing of, or continuing to use the recalled eye drops were not provided in the source material and are therefore unavailable here.
Frequently Asked Questions
Why were Clear Eyes eye drops recalled?
Clear Eyes Maximum Itchy Eye Relief eye drops were recalled because of potential contamination and a lack of assurance of sterility, according to the supplied FDA recall information.
Which Clear Eyes product is affected?
The recall affects 15mL bottles of Clear Eyes Maximum Itchy Eye Relief.
What is the recalled Clear Eyes lot code?
The supplied recall information identifies lot code 2552A.
What is the expiration date of the recalled Clear Eyes eye drops?
The expiration date listed for the recalled product is September 30, 2027.
What is the Clear Eyes recall number?
The recall number is D-0766-2026.
Was the Clear Eyes recall nationwide?
Yes. The supplied information states that the affected eye drops were distributed nationwide.
What does a Class II recall mean?
The supplied FDA definition states that a Class II recall involves a product that could cause temporary or medically reversible adverse health consequences.
Information Not Available in the Supplied Material
To preserve factual accuracy, the following details have not been added or inferred because they were not included in the original content:
- Specific consumer disposal or return instructions
- Retailer or store names
- Distribution dates
- Number of adverse events or complaints
- Specific contamination organism or substance
- Recommended medical treatment
- Consumer contact telephone number
- Manufacturer customer-service instructions
- Exact FDA notice publication URL
- Whether other Clear Eyes products or lot codes are affected
These details should only be added after verification from an authoritative source.
Disclaimer: This article is provided for informational purposes based on the supplied recall information. Readers should verify the latest recall information and instructions from the U.S. Food and Drug Administration before taking action.
MaalFreeKaa
Lead Researcher and Editor at MaalFreeKaa, specializing in global consumer rewards and brand launch offers for the USA, UK, and Canada. Since 2008, I have been dedicated to verifying legitimate freebies and international giveaways, providing first-hand proof and manual audits to ensure our community only accesses high-value, safe opportunities from top-tier global brands
