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FDA Urgently Warns: 26 Eye Drops Recalled Due to Potential Blindness Risk!

Posted on October 28, 2023 By Haley Bennett

The US Food and Drug Administration (FDA) has issued a severe warning to the public regarding certain over-the-counter eye drop products from popular brands. According to Reuters, these seemingly harmless eye drops, commonly used for treating dry eyes and eye irritation, have been linked to the potential risk of eye infections, which could result in partial vision loss or even blindness.

The brands involved in the warning include CVS Health Corp, Rite Aid, Cardinal Health, Target’s ‘up & up’ brand, and Velocity Pharma. While no adverse events have been reported at this time, the FDA’s actions indicate that these products could pose a significant threat to consumers. Upon investigating the manufacturing facilities of the implicated brands, the FDA found unsanitary conditions, leading to the recall of all the products in question.

CVS, Rite Aid, and Target have promptly responded by removing the affected products from their stores and websites. These brands have also committed to offering full refunds to customers who return the recalled eye drops. However, Leader, Rugby, and Velocity branded products may still be available for purchase, both in-store and online, despite the FDA’s concerns.

The eye drops under scrutiny are supposed to be sterile, as contamination in these products can have serious consequences. Ophthalmic drug products, specifically, pose a higher risk due to their direct application to the eyes, bypassing some natural defenses. The FDA advises consumers to promptly discard these products and seek medical attention if they experience any signs or symptoms of an eye infection after using the eye drops.

Although the FDA has not received any reports of adverse events related to these products, their urgent warning emphasizes the severity of the situation. In a separate warning earlier this month, the FDA cautioned eight companies, including CVS and Walgreens Boots Alliance, against manufacturing or marketing unapproved eye products.

To ensure the safety of medical products, the FDA encourages individuals who have been affected by these eye drops or suspect any quality problems or adverse events related to any medication to report their concerns through the FDA’s MedWatch Adverse Event Reporting program.

Please note that this article is protected by copyright and should not be reproduced without permission.

Tags: FDA, eye drops, eye infections, product recall, CVS, Rite Aid, Cardinal Health, Target, Velocity Pharma, sterile products, ophthalmic drug products, safety, MedWatch Adverse Event Reporting program.

Haley Bennett

I have over 10 years of experience in the cryptocurrency industry and I have been on the list of the top authors on LinkedIn for the past 5 years. I have a wealth of knowledge to share with my readers, and my goal is to help them navigate the ever-changing world of cryptocurrencies.

Health Tags:26, drops, eye, fda, issues, over, recalled, risk, urgent, warning

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