AvKARE Eye Drop, Ophthalmic Gel & Solution Injury Lawsuit Lawyer

National Law Firm Investigating AvKARE Eye Product Injuries

Parker Waichman LLP is currently reviewing legal claims from individuals who used AvKARE-manufactured or distributed eye drop products and subsequently suffered eye infections, inflammation, or vision complications. In April 2025, the U.S. Food and Drug Administration (FDA) announced a Class II nationwide recall involving over 1.8 million units of AvKARE eye drops, gels, and solutions. The products are being recalled due to serious concerns involving lack of sterility and manufacturing deviations that potentially expose users to harmful contaminants.

Our firm is offering free consultations to individuals across all 50 states who may have experienced adverse effects after using the affected AvKARE eye products. Our team is ready to investigate your situation, determine if your injuries may be connected to these recalled eye solutions, and pursue financial compensation if warranted.

What Are the AvKARE Eye Products?

The recall affects several products distributed under the AvKARE label, including artificial tears, ophthalmic solutions, gels, and lubricating eye drops. These items are used primarily to treat dry eye symptoms and other mild ocular conditions by providing artificial moisture to the surface of the eye.

Some of the affected products include:

• Artificial Tears Ophthalmic Solution (NDC# 50268-043-15)
• Carboxymethylcellulose Sodium Ophthalmic Gel 1% (NDC# 50268-066-15)
• Carboxymethylcellulose Sodium Ophthalmic Solution 0.5% (NDC# 50268-068-15)
• Lubricant Eye Drops Solution (NDC# 50268-126-15)
• Polyvinyl Alcohol Ophthalmic Solution 1.4% (NDC# 50268-678-15)

These products were shipped nationwide between May 2023 and April 2025 and were intended to relieve dry eye symptoms and general irritation.

What Conditions Are These Eye Drops Used to Treat?

AvKARE’s ophthalmic products are widely used to provide relief for symptoms associated with dry eye syndrome, a condition affecting millions of Americans. The symptoms may include stinging, burning, grittiness, and blurred vision. These products are also used by patients recovering from eye surgery, managing contact lens discomfort, or dealing with mild infections.

By lubricating the surface of the eye, these drops are supposed to prevent discomfort and support eye health. However, if these products are contaminated or not properly manufactured, they can introduce dangerous bacteria or other harmful substances directly into the eye, where they can do serious damage.

Why Were These Eye Drops Recalled?

According to the FDA and the recalling firm, BRS Analytical Services, LLC, the AvKARE eye drops were recalled due to deviations from Current Good Manufacturing Practices (cGMP) and a lack of assurance of sterility. When cGMP standards are violated, the safety and effectiveness of the drug cannot be guaranteed. In the case of sterile products such as eye drops, even minor manufacturing errors can allow contaminants into the product, potentially exposing users to eye infections and other complications.

The risk is compounded because many of the recalled eye drops were marketed as sterile and used by vulnerable populations, including the elderly and post-surgical patients. Although there have been no public reports of serious injury so far, the volume of recalled product and the nature of the violations suggest that there could be patients who were harmed but have not yet connected their symptoms to these products.

Potential Injuries and Adverse Effects Linked to Unsafe Eye Drops

If an eye drop product is not sterile, it can introduce harmful bacteria or irritants into the eye, leading to a range of mild to severe injuries. Potential complications include:

• Eye infections (bacterial conjunctivitis, keratitis)
• Blurred or impaired vision
• Redness, itching, or pain
• Swelling of the eyelids or surrounding tissue
• Eye discharge or crusting
• Corneal damage
• Permanent vision loss (in extreme cases)

Patients with compromised immune systems, recent eye surgeries, or underlying conditions may face heightened risk. If you’ve experienced unusual symptoms after using AvKARE-labeled eye products, you may be entitled to compensation.

Nationwide Legal Representation for Patients Injured by Contaminated or Unsafe Eye Drop Products

We are investigating injury claims from patients across the United States who may have suffered harm after using any of the recalled AvKARE eye drop or gel products. If your symptoms began shortly after using one of the recalled lots and required medical treatment, our legal team may be able to assist you.

Our firm will obtain your medical records, gather evidence regarding your eye product use, and work with qualified consultants to evaluate whether the recalled product may have caused your injuries. There is no cost to you unless we recover compensation on your behalf.

Why Work with Parker Waichman LLP?

• Decades of success in complex product liability and defective drug litigation
• National representation: we accept cases from all 50 states
• No out-of-pocket fees — we only get paid if we win your case
• Free and confidential consultations
• Extensive experience in FDA-regulated product cases

Parker Waichman LLP has recovered billions of dollars for clients harmed by unsafe consumer products and medications. Our legal team is prepared to fight for accountability and justice for injured victims of defective or unsanitary medical products.

AvKARE Eye Drop Injury Claim Frequently Asked Questions (FAQs)

What should I do if I used AvKARE eye drops and had eye problems?

Stop using the product immediately. Save the packaging and bottle, and seek medical attention if symptoms persist or worsen. Then, speak with an attorney to determine if your experience qualifies for legal action.

What evidence do I need to file a lawsuit?

Keep any unused product, packaging, or purchase receipts. Also keep documentation of your injuries, such as medical records, diagnoses, and prescriptions. Our law firm can assist in collecting and organizing this evidence.

Is there a time limit to file a lawsuit?

Yes. Each state has a statute of limitations that determines how long you have to bring a claim. The time limit usually begins when you discovered (or should have discovered) the injury. Contact us promptly to protect your rights. 

What damages can I recover in a defective eye drop lawsuit?

You may be eligible to recover compensation for medical bills, lost wages, pain and suffering, future healthcare costs, and other economic or personal losses resulting from your injuries.

Will I have to pay legal fees up front?

No. Parker Waichman LLP takes all eye drop recall cases on a contingency fee basis. That means there are no fees unless we recover money for you.

Contact Parker Waichman LLP For a Free Case Review

If you or someone you care about suffered eye infections, vision problems, or any other medical complications after using recalled AvKARE eye drops or ophthalmic products, you may be entitled to compensation. Our national defective product law firm is currently accepting cases nationwide. We can help determine if your injury qualifies for a lawsuit and pursue the recovery you deserve.

Call 800-968-7529 for a free and confidential case evaluation with Parker Waichman LLP. Regardless of your location or where your injury occurred, our nationwide product injury law firm is ready to assist you.