Clear Eyes Maximum Itchy Eye Relief eye drops and packaging, the product involved in the 2026 recall.

Clear Eyes Recall Lawsuit Lawyer

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Clear Eyes Maximum Itchy Eye Relief eye drops and packaging, the product involved in the 2026 recall.

Can I File a Lawsuit for an Injury Caused by Recalled Clear Eyes Eye Drops?

Possibly. If you used the recalled Clear Eyes Maximum Itchy Eye Relief and suffered an eye infection, vision problems, significant eye pain, or another injury, you may have a product liability claim. The recall itself does not establish that the product caused your injury; a claim requires evidence connecting the recalled product to the harm you suffered.

One of the most well-known and popular over-the-counter eye drops for redness relief, Clear Eyes Maximum Itchy Eye Relief, has been voluntarily recalled nationwide. The manufacturer, Prestige Brands Holdings, cited concerns about contamination and a lack of sterility in a specific batch. The recall affects nearly 40,000 bottles from that batch.

Dolman Law Group is investigating potential injury claims involving the recalled eye drops. If you developed an eye infection, vision problems, or another serious eye injury after using the recalled drops, save the bottle, packaging, and any proof of purchase. Our product liability lawyers can review what happened to you and explain your legal options in a free consultation.

2026 Clear Eyes Recall: Quick Facts

Recall InformationAffected Product
ProductClear Eyes Maximum Itchy Eye Relief
Bottle Size0.5 fl oz (15 mL)
Affected Lot2552A
Expiration Date09/30/2027
NDC67172-999-01
UPC6 78112 65920 3
Recall NumberD-0766-2026
Bottles Recalled39,060
DistributionNationwide in the United States
Recall InitiatedJuly 29, 2026
FDA ClassificationClass II
FDA Classification DateAugust 14, 2026
Reason for RecallLack of assurance of sterility due to potential contamination
Recalling FirmPrestige Brands Holdings
Recall StatusOngoing

What is a Class II Recall from the FDA?

An FDA Class II designation is a medium-risk classification. Although it’s not the highest classification, it doesn’t mean it’s unimportant or not dangerous. A Class II recall means the FDA has determined that use of or exposure to the recalled product may cause either temporary or adverse health consequences that are treatable.

What Contaminant Caused the Clear Eyes Eye Drop Recall? 

The FDA’s recall notice does not identify a specific contaminating organism or report a particular infection, injury, or death related to the recalled lot. 

We will continue to update this page as additional information about the recall, reported injuries, potential contaminants, and the development of potential Clear Eyes lawsuits becomes available.

man applying Clear Eyes eye drops to his eye, representing the Clear Eyes Maximum Itchy Eye Relief Recall - Dolman Law Group

Why Were Clear Eyes Maximum Itchy Eye Relief Drops Recalled?

Prestige Brands Holdings couldn’t verify that this batch of Clear Eyes Maximum Itchy Eye Relief was sterile, so the company recalled it. The FDA enforcement report points to potential contamination as the underlying concern.

Eye products can carry a higher risk of infection than products applied to the skin because the eye does not have the same protective barrier as skin. When a contaminated eye product is applied, bacteria, fungi, or other microorganisms can come into direct contact with sensitive eye tissue and potentially cause an infection.

What we learn next could significantly change our understanding of this recall. Additional information may reveal what caused the sterility concern, whether actual contamination has been identified, and whether the problem is limited to Lot 2552A or potentially affects other products or batches.

How Do I Know If My Clear Eyes Eye Drops Were Recalled?

Check the product name, bottle size, lot number, and expiration date on your Clear Eyes packaging. The current recall applies to a specific lot (aka batch) of Clear Eyes Maximum Itchy Eye Relief distributed nationwide.

Clear Eyes Recall Information Infographic Showing Where Lot and Expiration Number Is Found - Clear Eyes Recall - Dolman Law Group

Your product is part of the current FDA recall if it has ALL of the following information:

  • Product: Clear Eyes Maximum Itchy Eye Relief
  • Size: 0.5 fl oz (15 mL)
  • Lot number: 2552A
  • Expiration date: 09/30/2027
  • NDC: 67172-999-01
  • UPC: 6 78112 65920 3

The lot number and expiration date are particularly important because someone could have the same Clear Eyes product and bottle size without having a bottle from the recalled lot.

What Should I Do If I Used Recalled Clear Eyes Eye Drops?

If you used Clear Eyes Maximum Itchy Eye Relief from recalled Lot 2552A, you should take the following steps:

  • Stop using the recalled eye drops. Do not continue using the affected bottle, even if you have not experienced any problems.
  • Seek medical attention for eye problems. If you develop new or worsening symptoms, such as eye pain or vision changes, contact a healthcare provider right away. Tell them that you used recalled eye drops.
  • Keep the bottle, packaging, and proof of purchase. Do not throw away the affected bottle, box, or other packaging. These items may provide evidence of the product you used if you later pursue a legal claim.
  • Save purchase information. Receipts, online orders, pharmacy records, retailer histories, or financial records may help establish when and where you purchased the product.
  • Document what happened. Write down a simple timeline, including when you purchased the product, when your first symptoms appeared, and when you sought medical treatment. These details are important and can become much harder to remember months later.

What Symptoms Should Clear Eyes Users Watch For?

People who used recalled Clear Eyes Maximum Itchy Eye Relief should pay attention to new or worsening eye pain, discharge, vision changes, redness, irritation, or other unusual eye discomfort.

Possible warning signs of an eye infection or other eye problem can include:

  • Eye pain or significant discomfort
  • Red or irritated eyes
  • Unusual discharge
  • Blurred vision or other vision changes
  • Increased tearing
  • Sensitivity to light
  • Swelling or inflammation around the eye
  • Symptoms that continue to worsen instead of improving

Obviously, not all of these symptoms necessarily mean the recalled Clear Eyes caused the problem. After all, redness and irritation may have been the reason someone purchased an eye-relief product in the first place.

What matters is whether symptoms are new, unusually severe, persistent, or worsening after using the recalled drops.

Have Any Injuries Been Linked to the Recalled Clear Eyes Eye Drops?

No. The FDA’s recall does not currently identify any specific injuries, infections, vision loss, or deaths caused by the recalled Clear Eyes Maximum Itchy Eye Relief eye drops. 

This does not necessarily mean no adverse events have occurred. It means we do not currently have reliable evidence establishing any injuries. The recall is still extremely new classifed by the FDA as ongoing.

Additional information will likely emerge as products are removed from circulation, adverse events are reported, and regulators continue evaluating the sterility problem.

Dolman Law Group is monitoring the recall and investigating potential claims from people who suffered serious eye injuries after using the affected product.

Who May Qualify for a Clear Eyes Eye Drop Lawsuit?

People who used recalled Clear Eyes Maximum Itchy Eye Relief and suffered a significant eye infection, vision problem, or other medically documented injuries may have grounds to investigate a product liability claim. Whether someone actually has a viable claim will depend on individual facts and whether evidence can connect an injury to the recalled product.

Because this recall is so new, there is not yet an established set of court-approved eligibility criteria for Clear Eyes Eye Drop Lawsuits.

Attorneys investigating potential cases will likely consider questions such as:

  • Did you use Lot 2552A?
  • Can you document the product or purchase?
  • Did you develop an eye infection or other significant injury?
  • When did your symptoms begin relative to using the drops?
  • What did your doctors diagnose?
  • Did you require medication, specialist treatment, hospitalization, or another intervention?
  • Did laboratory or culture testing identify an infection?
  • Can medical and scientific evidence connect the injury to the recalled product?

Medical records will be important because they can help establish the diagnosis, severity, and progression of an injury, as well as whether medical evidence supports a connection to the recalled product.

Exactly what evidence will be necessary to prove causation will also become clearer as investigators learn more about the recall.

Who Could Be Liable for Injuries Caused by Recalled Clear Eyes Eye Drops?

Companies responsible for manufacturing, distributing, or selling a defective ophthalmic product may potentially face liability when a product causes an injury. 

The FDA identifies Prestige Brands Holdings as the recalling firm, while the recalled product is labeled as distributed by Medtech Products Inc., a Prestige Consumer Healthcare company.

Determining which entity is legally responsible requires more than just looking at the Clear Eyes name on the bottle.

An investigation will examine the companies involved in manufacturing the drops; the supplier of the bottles and components; the company filling and packaging the product; the company responsible for performing quality-control testing; and the distributor of the eye drops.

Important questions surrounding the potential problems related to the recalled eye drops:

  • Where and how was the recalled product manufactured?
  • What caused the lack of assurance of sterility?
  • Were appropriate procedures used to prevent microbial contamination?
  • Did manufacturing or quality-control processes fail?
  • When did the responsible companies learn about the potential problem?
  • What actions were taken after the problem was discovered?
  • Can a product defect be connected to consumers’ injuries?

At this stage, these are investigative questions; more information and investigation are still necessary to understand what is going on with Clear Eyes eye drops.

Depending on what an investigation uncovers and which state’s law applies, potential legal claims against Prestige Brands Holdings, Medtech Products Inc., and Prestige Consumer Healthcare could include:

  • Manufacturing defect
  • Negligence
  • Failure to warn
  • Breach of warranty
  • Potential state-specific product liability laws
Woman rubbing irritated eyes while sitting at home, illustrating symptoms relevant to the Clear Eyes eye drop recall.

What Compensation Could Be Available in a Clear Eyes Eye Drop Lawsuit?

Someone who suffers a serious injury caused by defective or contaminated eye drops may be able to seek compensation for any financial losses and personal harm that resulted from their injuries.

Depending on the individual details of the case and state laws, damages may include:

  • Past and future medical expenses
  • Lost income
  • Reduced future earning capacity
  • Pain and suffering
  • Permanent vision impairment
  • Out-of-pocket expenses related to the injuries
  • Wrongful death damages, if applicable
  • Punitive damages, if deemed appropriate

The compensation and damages in cases like this will vary considerably from one person to another depending on the severity of their situation and the amount of suffering caused. 

All of this is, of course, dependent on whether the manufacturers and/or other parties are found to be responsible for any contamination of Clear Eyes Maximum Itchy Eye Relief eye drops and whether or not injuries occurred. 

How Much Could a Clear Eyes Eye Drop Lawsuit Be Worth?

It is far too early to responsibly estimate the value of a Clear Eyes eye drop lawsuit. There are currently no settlements, verdicts, bellwether results, or other reliable benchmarks we can use to estimate what these cases may eventually be worth.

Any specific settlement figures you see online right now are speculation and irresponsible.

If the facts develop in a way that makes lawsuits feasible, their value will ultimately depend on the strength of the evidence, the culpability of the parties involved, and the severity and long-term consequences of each person’s injuries, as we have already mentioned in this article. 

A temporary infection that resolves with treatment, for example, would be a very different case (if it would be a case at all) from one involving permanent corneal damage or significant vision loss.

How Long Do You Have to File a Clear Eyes Eye Drop Lawsuit?

The deadline for filing a Clear Eyes lawsuit depends on the applicable statute of limitations in each state for the type of case this turns out to be.

Product liability statutes of limitations vary by state, and when that filing deadline begins can also vary depending on when the injury occurred and, in some jurisdictions, when the person discovered, or reasonably should have discovered, its potential cause.

There is not one nationwide Clear Eyes filing deadline.

The July 29 recall initiation and August 14 FDA classification are important dates, but neither automatically establishes the statute of limitations for potential lawsuits.

If you suffered a significant injury and believe it was related specifically to Clear Eyes Maximum Itchy Eye Relief, you should not wait for a class action, MDL, or some announcement of a settlement before investigating a potential claim. There may never be an MDL or class action involving this recall, and ordinary legal deadlines continue to run regardless of whether some coordinated litigation develops.

Clear Eyes Recall Lawsuit Updates

The Clear Eyes Maximum Itchy Eye Relief recall is ongoing, and the regulatory and potential litigation picture may change quickly. We will update this timeline as the FDA releases additional information, injuries are reported or confirmed, lawsuits are filed, or other significant developments occur.

August 14, 2026: FDA Classifies the Clear Eyes Recall as Class II

The FDA officially classified the recall of Clear Eyes Maximum Itchy Eye Relief as a Class II recall on August 14, 2026.

The FDA continues to list the recall as ongoing and identifies the reason as a lack of confidence in the sterility of the product due to potential contamination concerns.

At this time, the FDA enforcement report has not identified a specific contaminant or confirmed any particular injuries related to the specific lot/batch of eye drops.

July 29, 2026: Prestige Brands Holdings Initiates Nationwide Clear Eyes Recall

Prestige Brands Holdings initiated a voluntary recall of 39,060 bottles of Clear Eyes Maximum Itchy Eye Relief on July 29, 2026.

The recall applies to 0.5 fl oz (15 mL) bottles from Lot 2552A, with an expiration date of September 30, 2027. The affected drops were distributed nationwide.

The FDA enforcement report states that the recall was initiated because of potential contamination and a lack of assurance of sterility. The FDA record also indicates that the company initially notified consignees or the public by letter and that a public press release was not issued.

What Happens Next With the Clear Eyes Recall?

Several important questions remain unanswered. Dolman Law Group will be watching for additional information concerning:

  • The reason sterility could not be assured
  • Whether testing confirms contamination in affected bottles
  • The identity of any microorganism or other contaminant discovered
  • Adverse events potentially associated with the recalled lot
  • Additional Clear Eyes products or lots added to the recall
  • Changes to the FDA recall status or classification
  • Lawsuits filed by injured consumers
  • Any coordinated federal litigation that may develop
Attorneys Stan, Becky, and Matt of Dolman Law Group

How Dolman Law Group Can Help With a Clear Eyes Recall Lawsuit

Dolman Law Group has extensive experience representing people injured by defective products and pursuing complex litigation against major corporations. These cases require much more than showing that someone was hurt.

If you were harmed by a recalled Clear Eyes product, we can help by:

  • Confirming whether the product came from recalled Lot 2552A
  • Preserving the bottle, packaging, and remaining contents
  • Establishing when and where the product was purchased
  • Reviewing medical records and the timing of symptoms
  • Identifying the diagnosis and extent of the injury
  • Reviewing laboratory or culture results when available
  • Investigating the companies involved in manufacturing and distributing the product
  • Monitoring FDA findings concerning the sterility problem
  • Evaluating medical and scientific causation
  • Calculating financial and personal losses
  • Protecting the claim before applicable filing deadlines expire

Large manufacturers and distributors have lawyers, experts, insurers, and substantial financial resources available to defend claims. An injured consumer should have a legal team capable of developing the other side of that case.

Experience Handling Defective Product and Mass Tort Litigation

Dolman Law Group handles complex product liability and mass tort claims involving defective drugs, medical products, consumer products, and other products alleged to have caused serious injuries.

These cases can raise complicated questions about manufacturing, corporate knowledge, regulatory compliance, medical causation, scientific evidence, and the responsibility of multiple companies involved in bringing a product to market.

When multiple people report similar injuries from the same product, litigation may eventually be coordinated through multidistrict litigation or other procedures. Our attorneys understand how large-scale product litigation can develop while continuing to focus on the evidence and damages specific to each individual client.

We Have the Resources to Take On Large Corporations

A defective-product case can require extensive investigation long before a jury ever hears about it. Depending on what the Clear Eyes investigation ultimately reveals, developing a claim could require obtaining corporate and regulatory records, examining manufacturing and quality-control evidence, working with medical and scientific experts, reviewing laboratory findings, establishing product identification, and connecting an individual injury to the alleged defect.

Dolman Law Group has experience litigating against major corporations and insurance companies with substantial resources available to aggressively defend claims. We are prepared to invest the time and resources necessary to investigate complex product liability cases rather than expecting an injured consumer to prove the case alone.

Talk to a Clear Eyes Recall Lawyer About Your Potential Claim

If you experienced a significant eye injury after using recalled Clear Eyes Maximum Itchy Eye Relief, a lawyer can evaluate whether you may have grounds for a product liability claim. You do not need to determine on your own whether the recalled product caused your injury before seeking legal advice.

During a free consultation, Dolman Law Group can review the circumstances of your injury, assess the available evidence, and explain whether pursuing a claim may be appropriate. The firm does not charge attorney’s fees unless it recovers compensation for you.

Frequently Asked Questions About the Clear Eyes Recall and Potential Lawsuits

Are all Clear Eyes eye drops being recalled?

No. The current recall applies to a specific lot of Clear Eyes Maximum Itchy Eye Relief. Other Clear Eyes products and lots are not currently identified as part of this recall.

Is the Clear Eyes recall likely to expand to other products or lots?

It is possible, but there is currently no evidence that the recall extends beyond the identified product and lot. If the FDA identifies additional affected products or lots, the recall information may be updated.

What does a Class II Clear Eyes recall mean?

A Class II recall means use of or exposure to the recalled product may cause temporary or medically reversible adverse health consequences, or that the likelihood of serious adverse health consequences is remote. A Class II classification does not mean that everyone who used the product will be injured.

What if I already threw away my Clear Eyes bottle?

You may still be able to document that you purchased or used the recalled product. Purchase records, pharmacy or retailer records, photographs, financial records, and medical records may help establish what product you used and what happened afterward.

Have recalled Clear Eyes drops caused blindness or vision loss?

The FDA’s current recall information does not state that the recalled Clear Eyes drops have caused blindness or vision loss. Serious eye injuries can occur with contaminated ophthalmic products, but injuries involving past product recalls should not be attributed to Clear Eyes without clear evidence.

Has the FDA identified what contaminated the Clear Eyes eye drops?

Not at this time. The FDA’s recall only identifies a lack of assurance of sterility and potential contamination. It does not identify a specific type of bacteria, fungus, or other contaminant.

Is there a Clear Eyes class action lawsuit?

No. There is currently no established Clear Eyes class action, multi-district litigation (MDL), or nationwide settlement program that consumers should assume they need to join. Because the recall is new, the potential for legal options could change as more information becomes available.

Do I have to wait for an MDL or class action before filing a Clear Eyes lawsuit?

No. An MDL or class action is not required before an attorney can investigate an individual product liability claim. Whether an individual lawsuit is appropriate depends on the person’s injuries, circumstances, and available evidence.

Can I file a lawsuit if I used recalled Clear Eyes but wasn’t injured?

Simply using a recalled product does not necessarily create a personal injury claim. A claim seeking compensation for physical harm generally requires an actual injury and evidence connecting that injury to the product.

Do I need a receipt to file a Clear Eyes lawsuit?

Not necessarily. A receipt can help establish that you purchased the product, but other records—such as online order histories, pharmacy or retailer records, photographs, financial records, and medical documentation—may also help establish product use.

How much is a Clear Eyes lawsuit worth?

It is too early to estimate potential Clear Eyes settlement values. There are currently no established settlements, verdicts, or settlement formulas for this recall, and the value of an individual claim would depend on factors such as the nature and severity of the injury and available evidence.

How much does it cost to hire Dolman Law Group for a Clear Eyes lawsuit?

Dolman Law Group offers free consultations for potential Clear Eyes injury claims. If the firm accepts your case, you pay no attorney’s fees unless the firm obtains compensation for you.


Sources

Matthew Dolman, Esq.
Legally Reviewed by

Matthew Dolman, Esq.

Founding Partner • Dolman Law Group Accident Injury Lawyers, PA
National Civil Trial Attorney

Matt Dolman is a Florida civil trial attorney with more than two decades of experience representing individuals in serious injury and wrongful death matters. His practice is built on disciplined case preparation, strategic litigation, and a clear understanding of how insurers evaluate claims. Dolman Law Group has secured more than $700 million in recoveries for clients. Matt is recognized by Super Lawyers, Florida Legal Elite, and Best Lawyers, and is a Lifetime Member of both the Million Dollar and Multi-Million Dollar Advocates Forums.

Florida Bar Member in Good Standing

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