Alcon Laboratories has issued a voluntary recall of one lot of Systane Lubricant Eye Drops Ultra PF, Single Vials On-the-Go, 25 count due to the risk of fungal contamination. This recall impacts Lot 10101, with an expiration date of September 2025, distributed across the United States through retail stores and online platforms. The recall follows a consumer report of foreign material found in a sealed vial, which testing revealed to be fungal in nature. Although no injuries or adverse reactions have been reported at this time, fungal contamination in an ophthalmic product presents significant health risks that cannot be overlooked.
Details of the Recall
The recalled product is packaged in 25-count boxes containing single-use vials. Consumers can identify the affected lot by checking the packaging for the lot number “10101” and looking for the green and pink carton with the “Systane” and “ULTRA PF” brand names.
Fungal contamination of an eye drop product is particularly concerning, given the delicate nature of the eye and the potential severity of resulting infections. While Alcon has not received reports of injuries linked to this lot, the company is taking proactive steps to remove potentially harmful products from circulation. Consumers are encouraged to contact Alcon Laboratories at 1-800-241-5999 with any questions or concerns about the recall.
Understanding the Risks of Contaminated Eye Drops
Using contaminated eye drops can introduce harmful microorganisms directly into the eye, potentially leading to fungal or bacterial infections. Fungal infections, while rare, can result in serious eye conditions such as keratitis (inflammation of the cornea), which may cause symptoms like redness, pain, blurry vision, or sensitivity to light. If untreated, these infections can escalate into severe complications, including corneal scarring, vision loss, or even the need for surgical interventions like corneal transplants.
Immunocompromised individuals face heightened risks. For these patients, a fungal infection can progress beyond the eye, potentially leading to systemic infections that may become life-threatening. Even healthy individuals should take these risks seriously, as fungal eye infections can develop rapidly and become difficult to treat. Prompt medical attention is crucial if you notice any unusual symptoms after using an affected product. Stopping the use of the recalled eye drops and consulting a healthcare professional are critical first steps to ensuring your health and safety.
The Need to Consult an Attorney if Harm Occurs
If you or someone you know has experienced harm or complications as a result of using a defective or recalled product, it is essential to consult an experienced product liability attorney. Manufacturers of medical products are legally obligated to ensure their items meet strict safety and quality standards before they reach consumers. When these standards are breached, and unsafe products cause harm, victims have the right to pursue compensation for medical expenses, pain and suffering, lost wages, and other damages.
Navigating the legal system in product liability cases can be complex. An attorney experienced in these matters can help investigate your case, gather evidence, and advocate on your behalf. Whether you suffered an eye infection, vision loss, or another adverse outcome, your attorney can determine whether the manufacturer’s negligence contributed to your injuries and guide you through the process of seeking justice.
Additionally, filing a claim not only helps you secure compensation but also holds manufacturers accountable. This accountability can drive improvements in safety protocols and prevent similar incidents from harming others. If you believe you have been affected by this recall, do not delay in seeking legal advice. An attorney can provide clarity on your rights, options, and next steps to ensure your interests are fully protected.
Steps for Affected Consumers
If you have purchased Systane Lubricant Eye Drops Ultra PF, Single Vials On-the-Go, check the lot number on your packaging. If it matches Lot 10101, stop using the product immediately and return it to the place of purchase for a refund or replacement. For further assistance, you can contact Alcon Laboratories at 1-800-241-5999 during business hours. If you suspect you have experienced any adverse effects, seek medical attention promptly and report your experience to the FDA’s MedWatch Adverse Event Reporting program. By staying informed and taking action, you can protect yourself and contribute to efforts to improve the safety of healthcare products for all consumers.
If you or a loved one has suffered harm due to this or any other defective product, you may have legal options to seek compensation for your injuries. Manufacturers have a responsibility to ensure their products meet stringent safety and quality standards. When they fail to do so, affected consumers have the right to hold them accountable. At Spagnoletti Law Firm, our lawyers can guide you through the process of obtaining the justice and compensation you deserve.
Contact Spagnoletti Law Firm at 713-804-9306 for a free consultation to discuss your case. Our experienced team is dedicated to protecting your rights and advocating for your best interests. Don’t delay—reach out today to ensure your voice is heard and your health is safeguarded.