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Parker Waichman LLP is actively reviewing legal claims on behalf of individuals who may have been harmed by unsterile eye drops distributed by AvKARE. More than 1.8 million cartons of various eye treatment products were recalled nationwide due to concerns over sterility. Improperly sterilized eye drops can cause serious infections, potentially leading to vision loss or permanent blindness. If you or someone you care about experienced medical complications after using AvKARE eye products, you may have grounds to file a product liability lawsuit.
As a national defective medical product law firm, we serve clients in all 50 states. Our attorneys are prepared to investigate these cases and pursue compensation for patients who were put at risk by unsafe eye drops.
AvKARE distributes a variety of ophthalmic products intended to relieve dry eye symptoms.
These include:
These products are typically used by people suffering from dry eye, which can cause irritation, stinging, burning, and blurred vision. For many, these drops are used daily and are considered a safe, over-the-counter remedy. However, when contamination is present, the risk of eye infection becomes significant.
Dry eye syndrome is a common condition where the eyes do not produce enough moisture or tears to stay properly lubricated. It can result from environmental factors, allergies, medications, and aging. The condition often causes discomfort, redness, light sensitivity, and difficulty focusing.
Eye drops, gels, and solutions are designed to provide temporary relief by supplementing natural tear production. Many patients rely on these products during allergy season or while using medications that dry out the eyes. The AvKARE products were marketed to treat these symptoms and were intended for safe, regular use.
According to both AvKARE and the FDA, the recall was initiated after a manufacturing audit revealed a lack of assurance regarding product sterility. While no specific contaminant was identified publicly, the announcement raised concerns that these products could be of “unacceptable quality.”
Any product used in the eyes must be manufactured under strict sterile conditions. When contamination is possible, the risk of infection rises dramatically. Eye infections linked to tainted drops may include corneal ulcers, conjunctivitis, and bacterial keratitis. In severe cases, these infections can result in permanent damage to the eye or vision loss.
Although no consumer injuries have been publicly confirmed so far, the scope of the recall — affecting 1.8 million cartons — indicates widespread distribution of potentially unsafe medication.
The most serious consequence of using contaminated eye drops is infection, leading to blindness. Other potential injuries and complications include:
The injuries caused by unsterile eye drops can progress rapidly. In past contamination cases, patients were hospitalized, required surgical intervention, and in some instances, suffered irreversible blindness.
If you used one of the recalled AvKARE eye products and suffered an eye infection, vision loss, or other related complications, you may be eligible to file a legal claim. Our firm is currently reviewing reports from across the country and working with medical experts to evaluate the risks.
We handle every aspect of the legal process, from collecting your medical records and product information to identifying whether a defective or unsterile batch was responsible for your injury. There are no upfront costs. We only get paid if we win your case.
Parker Waichman LLP has decades of experience holding pharmaceutical and medical device companies accountable for defective products. If you were harmed, we can help.
We are here to fight for those who trusted a product to improve their health and suffered serious harm instead.
What symptoms should I watch for if I used AvKARE eye drops?
If you used one of the recalled eye drop products, monitor for signs of infection such as eye redness, pain, swelling, blurred vision, discharge, or increased sensitivity to light. Any sudden changes in your vision should prompt immediate medical evaluation.
What should I do if I still have the recalled eye drops?
Stop using them immediately and keep the packaging, if possible. Do not discard the product until you’ve spoken with a medical professional and a legal team. This can serve as valuable evidence if you choose to file a claim.
Can I file a lawsuit if I haven’t lost vision but needed treatment?
Yes. Even if your infection was treated and your vision returned to normal, you may still be entitled to compensation. Lawsuits may cover medical expenses, missed work, pain and suffering, and more.
Is there a time limit to file a claim?
Yes. Each state sets a deadline, known as a statute of limitations, for filing personal injury claims. This is typically between one and three years. Contacting a law firm as soon as possible protects your right to file.
How do I begin the process?
You can start by calling Parker Waichman LLP for a free consultation. Our team will listen to your experience, evaluate your potential claim, and guide you on the next steps. We make it as easy and stress-free as possible.
If you or a loved one has experienced vision problems, eye infections, or permanent damage after using a recalled AvKARE eye drop product, contact Parker Waichman LLP today. Our nationwide product injury law firm is actively representing individuals across the country in lawsuits involving unsafe pharmaceutical products.
We offer free consultations and never charge fees unless we win your case. Call 800-968-7529 now to speak with a legal representative who can help you understand your rights.
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