One of the most popular over-the-counter eye drops for redness relief, Clear Eyes Maximum Itchy Eye Relief, has been recalled nationwide due to concerns about contamination and a lack of sterility. The recall currently affects nearly 40,000 bottles of the eye drops from a specific batch.
The manufacturer of Clear Eyes Maximum Itchy Eye Relief, Prestige Brands Holdings, initiated a voluntary recall of its product on July 29, 2026; the FDA officially classified it as a Class II recall on August 14, 2026.
If you have used Clear Eyes Maximum Itchy Eye Relief and developed an eye infection, vision problems, significant eye pain, or any other serious injury, you may have been affected by the unsterile eye drops in question. If you still can, save the bottle and packaging; the lot number could become important evidence in determining whether you used the recalled eye drops.
Dolman Law Group is currently investigating potential injury claims involving the recalled Clear Eyes Maximum Itchy Eye Relief eye drops.
Our product liability lawyers have extensive experience with defective products, medicines, exposures, and litigation with some of the biggest corporations and entities in the world. We will review your case at no cost and help determine whether your injuries may be connected to the recalled eye drops.
CLEAR EYES RECALL ALERT
Status: RECALL ONGOING
Affected Product: Clear Eyes Maximum Itchy Eye Relief, 0.5 fl oz (15 mL)
Recalled Lot: 2552A | Expiration: 09/30/2027
Reason for Recall: Lack of assurance of sterility due to potential contamination.
Used the recalled drops and suffered an injury? Stop using the product, preserve the bottle and packaging, and seek medical attention for concerning symptoms.
Last updated: August 16, 2026
Quick Answer: Which Clear Eyes Eye Drops Were Recalled?
The 2026 Clear Eyes recall currently involves one lot (batch) of 0.5 fl oz (15 mL) Clear Eyes Maximum Itchy Eye Relief: Lot 2552A, with an expiration date of September 30, 2027.
The FDA initiated the recall due to uncertainty about the sterility of the product because of potential contamination.
*This recall does not currently include all Clear Eyes products or every bottle of “Maximum Itchy Eye Relief.”
2026 Clear Eyes Recall: Quick Facts
| Recall Information | Affected Product |
|---|---|
| Product | Clear Eyes Maximum Itchy Eye Relief |
| Bottle Size | 0.5 fl oz (15 mL) |
| Affected Lot | 2552A |
| Expiration Date | 09/30/2027 |
| NDC | 67172-999-01 |
| UPC | 6 78112 65920 3 |
| Recall Number | D-0766-2026 |
| Bottles Recalled | 39,060 |
| Distribution | Nationwide in the United States |
| Recall Initiated | July 29, 2026 |
| FDA Classification | Class II |
| FDA Classification Date | August 14, 2026 |
| Reason for Recall | Lack of assurance of sterility due to potential contamination |
| Recalling Firm | Prestige Brands Holdings |
| Recall Status | Ongoing |
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?
At this point, 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.
This is an important piece of information that is missing.
We will continue updating this page as additional information about the recall, reported injuries, potential contaminants, and the development of potential Clear Eyes lawsuits as information becomes available.
Why Were Clear Eyes Maximum Itchy Eye Relief Drops Recalled?
This particular batch of Clear Eyes Maximum Itchy Eye Relief was recalled because the sterility of the affected product could not be assured.
According to the FDA enforcement report, the recall is due to potential contamination.
Products applied to the eye have a much higher risk of infection than other topical products, such as those applied to the skin. Unlike your eyes, your skin acts as a thick, waterproof barrier that keeps germs out; the eyes, however, are delicate, exposed organs made of living tissue.
When a contaminant is introduced directly to the surface of the eye, it bypasses most of the body’s primary defenses, creating an immediate pathway for dangerous pathogens to multiply and reach critical areas of your body.
Because eye drops are frequently used on compromised or irritated eye tissue, any introduction of bacteria, fungi, or viruses can rapidly escalate into severe, sight- and possibly life-threatening complications.
This is why the FDA requires ophthalmic drugs to be sterile. Eye drops are applied directly to the surface of the eye, where contamination can bypass some of the body’s natural defenses against infection. The risk can become even greater when the surface of the eye is already irritated or damaged, creating an opportunity for microorganisms to cause an infection.
Depending on the type of microorganism and severity of the infection, contaminated ophthalmic products can potentially cause serious complications involving the cornea and other structures of the eye. Previous contaminated eye drop incidents demonstrate that, in severe cases, these infections can threaten a person’s vision.
It does not mean the FDA has officially confirmed that bottles of the recalled Clear Eyes product contain dangerous bacteria or fungi.
The FDA enforcement report currently describes the problem as a “lack of assurance of sterility” and cites “potential contamination.”
It does not identify a specific microorganism or explain exactly how the potential contamination occurred. Something caused the company to lose confidence that this particular batch met the sterility requirements for an ophthalmic product, but we do not yet know what that was. More information may eventually explain whether the concern originated with the bottles, manufacturing process, testing, packaging, or another part of production.
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.
Past Recalls Show Why Sterility Is So Important in Ophthalmic Products
Past recalls involving other ophthalmic products demonstrate why the FDA takes sterility problems with eye drops so seriously. Contaminated eye drops have previously been associated with serious infections, corneal damage, vision loss, and, in the most severe cases, blindness.
These previous recalls have involved problems like bacterial or fungal contamination, manufacturing conditions that created a risk of contamination, and packaging defects that could compromise sterility.
They involved different products, manufacturers, and circumstances, so they are not evidence that recalled Clear Eyes drops have caused the same injuries.
However, we do not yet know what the contamination is, if any, or what injuries, or their severity, have been reported.
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.
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, stop using the affected bottle immediately and pay attention to any new or worsening eye symptoms.
If you believe you have already developed an infection or another eye injury after using the affected drops, seek medical attention right away.
You should also make sure to keep the bottle rather than throw it away, in case it’s needed as evidence later.
Steps to Take If You Used Recalled Clear Eyes Eye Drops
If you used the recalled drops:
- Stop using the recalled bottle. Set it aside somewhere it cannot accidentally be used again.
- Preserve the bottle and packaging if you experienced an injury. Keep the bottle, cap, box, and remaining contents.
- Photograph the product information. Take clear pictures of the lot number, expiration date, UPC, NDC, bottle, and packaging.
- Seek medical attention for concerning symptoms. Eye pain, vision changes, persistent redness or irritation, or worsening symptoms should be evaluated by an appropriate healthcare professional.
- Tell your healthcare provider what you used. If known, tell them your bottle came from recalled Lot 2552A.
- Save purchase information. Receipts, online orders, pharmacy records, retailer histories, or financial records may help establish when and where you purchased the product.
- Write down a simple timeline. Record approximately when you purchased and began using the drops, when you last used them, when symptoms first appeared, and when you sought medical treatment. These details can become much harder to remember months later.
What If I Already Threw Away the Bottle?
Not having the bottle does not automatically eliminate a potential claim, although it can make identifying the exact product and lot more difficult.
Other evidence may include online purchase history, like information kept in an app’s Recent Purchases section, emailed receipts, pharmacy or retailer records, potential photographs, bank statements, and medical records identifying the eye drops you reported using.
What Are Potential Complications Associated with Contaminated Eye Drops?
As we discussed earlier, contaminated eye drops can be particularly dangerous because they are applied directly to the eye, bypassing some of the body’s natural defenses against infection.
Depending on the type and severity of an infection, potential complications can include:
- Serious eye infections
- Microbial keratitis and other corneal infections
- Corneal ulcers
- Corneal damage or scarring
- Permanent vision impairment
- Partial or complete vision loss
- Infection that spreads beyond the eye
Serious infections may require prescription medications and continued treatment from an ophthalmologist or other specialist. Infections involving the cornea can potentially cause permanent vision damage, while an infection that spreads into the bloodstream can become much more serious and affect the entire body.
Again, the FDA has not linked these complications to the currently recalled batch of Clear Eyes eye drops.
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?
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.
It also does not identify a particular bacterium, fungus, or other contaminant in the affected batch of eye drops.
However, that does not necessarily mean no adverse events have occurred. It means we do not currently have reliable evidence establishing that they have.
The recall is still extremely new. Prestige Brands Holdings initiated it on July 29, 2026; the FDA classified it on August 14, and this article is being published for the first time on August 16, 2026.
The FDA currently classifies the recall 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 the individual facts and whether evidence can connect the 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 particularly 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 become clearer as investigators learn why sterility could not be assured, whether contamination is confirmed, what contaminant may be involved, and whether similar injuries are being reported among other users of the same eye drops.
Who Could Be Liable for Injuries Caused by Recalled Clear Eyes Eye Drops?
Companies responsible for manufacturing, distributing, or selling a defective ophthalmic product could potentially face liability when the 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.
What Are The Potential Legal Claims Against Clear Eyes?
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
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.
We 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
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. Our attorneys investigate what went wrong with the product, identify the companies responsible, develop medical and scientific evidence, and pursue compensation for the injuries and losses our clients suffered.
That experience can become particularly important when a consumer-product recall develops into complex litigation.
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 involve 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 large numbers of people allege similar injuries from the same product, cases may eventually be coordinated through multidistrict litigation or other procedures. Our attorneys understand how large-scale product litigation develops 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.
How We Would Investigate a Potential Clear Eyes Claim
Our investigation may include:
- 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
As the recall develops, additional evidence may tell us considerably more about what caused the sterility problem and whether consumers suffered similar injuries.
Talk to a Clear Eyes Recall Lawyer About Your Potential Claim
If you developed a serious eye infection, vision problems, or another significant injury after using recalled Clear Eyes Maximum Itchy Eye Relief, Dolman Law Group can investigate whether you may have a product liability claim.
You do not need to know whether contamination caused your injury before contacting us. Determining causation is part of the investigation.
If you still have the bottle, do not throw it away. Preserve the product and packaging, gather whatever purchase and medical records you can easily locate, and contact Dolman Law Group for a free case evaluation.
Our attorneys can review what happened, determine whether your bottle was included in the recall, evaluate the available medical evidence, and explain your legal options.
There is no fee for the initial consultation, and you do not pay attorney’s fees unless we recover 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 specifically to Clear Eyes Maximum Itchy Eye Relief, 0.5 fl oz (15 mL), Lot 2552A, with an expiration date of September 30, 2027. The FDA enforcement report does not currently identify other Clear Eyes products 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 this recall will expand beyond Clear Eyes Maximum Itchy Eye Relief Lot 2552A. Sterility-related recalls can sometimes expand if an investigation finds that the underlying problem affected additional production lots, products, or products manufactured under the same conditions.
For now, consumers should rely on the FDA’s current recall information rather than assuming that other Clear Eyes or Prestige Consumer Healthcare products are affected. We will update this page if the FDA identifies additional products or lots.
Why were Clear Eyes eye drops recalled?
The affected lot was recalled because of a lack of assurance of sterility due to potential contamination. The FDA’s current enforcement report does not identify a specific contaminant or explain what caused the sterility problem.
What lot number of Clear Eyes Maximum Itchy Eye Relief was recalled?
The recalled lot is 2552A, with an expiration date of 09/30/2027. The affected product is a 0.5 fl oz (15 mL) bottle with NDC 67172-999-01 and UPC 6 78112 65920 3.
What does a Class II Clear Eyes recall mean?
A Class II recall generally means the FDA has determined that use of or exposure to the product may cause temporary or medically reversible adverse health consequences or that the probability of serious adverse health consequences is remote.
What should I do with recalled Clear Eyes eye drops?
Stop using the affected bottle. If you experienced an injury after using it, preserve the bottle, remaining contents, cap, and packaging and seek appropriate medical care for concerning symptoms.
Should I throw away my recalled Clear Eyes bottle?
If you believe you were injured after using the recalled drops, do not throw the bottle away. The product and its identifying information could become important evidence.
What if I already threw away my Clear Eyes bottle?
You may still be able to investigate a potential claim. Purchase histories, pharmacy or retailer records, photographs, financial records, receipts, and medical records may help establish which product you used.
What symptoms should I watch for after using recalled Clear Eyes?
Watch for new or worsening symptoms such as eye pain, redness or irritation, unusual discharge, blurred vision or other vision changes, sensitivity to light, swelling, or significant discomfort. Seek appropriate medical attention for concerning symptoms.
Have recalled Clear Eyes drops caused blindness or vision loss?
The FDA’s current enforcement report does not state that the recalled Clear Eyes drops have caused blindness, vision loss, or another specific injury. Severe injuries have occurred with other contaminated ophthalmic products, but those incidents should not be attributed to Clear Eyes without supporting evidence.
Has the FDA identified what contaminated the Clear Eyes eye drops?
Not at this time. The FDA enforcement report identifies potential contamination and a lack of assurance of sterility, but it does not identify a specific bacterium, fungus, or other contaminant.
Is there a Clear Eyes class action lawsuit?
There is currently no established Clear Eyes class action, MDL, or nationwide settlement program involving this 2026 recall that consumers should assume they must join. The recall is extremely new, and the litigation picture may change as additional information becomes available.
Do I have to wait for an MDL or class action before filing a Clear Eyes lawsuit?
No. Someone with a significant injury does not need to wait for an MDL or class action before having an attorney investigate an individual product liability claim.
Can I file a lawsuit if I used recalled Clear Eyes but wasn’t injured?
Simply purchasing or using a recalled product is different from having a personal injury claim seeking compensation for physical harm. A product liability claim generally requires an actual injury and evidence connecting that injury to the allegedly defective product.
Do I need a receipt to file a Clear Eyes lawsuit?
Not necessarily. A receipt can be useful, but online orders, pharmacy records, retailer accounts, photographs, financial records, and medical documentation may also help establish the product purchase and use.
How much is a Clear Eyes lawsuit worth?
It is too early to responsibly estimate Clear Eyes settlement values. There are currently no established settlements, verdicts, or settlement matrix for this recall.
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 we accept your case, you pay no attorney’s fees unless we obtain compensation for you.
