Hearst Magazine Media, Inc. All Rights Reserved. 24/7 coverage of breaking news and live events. TO DATE ALTAIRE HAS NOT OBTAINED ANY OUT OF SPECIFICATIONS RESULTS, INCLUDING IN-HOUSE AND THIRD PARTY STERILITY TESTING, FOR THE PRODUCTS. First published on March 8, 2023 / 5:32 PM. The outbreak has also been connected to eight recent reports of vision loss and four reports of enucleation, or surgical removal of an eyeball. Brimonidine Tartrate Ophthalmic Solution, 0.15%. Refresh Plus ophthalmic (eye): Uses, Side Effects, Interactions - WebMD The deadly bacteria linked to recalled eyedrops causing infection and blindness had never been seen in the U.S. until 2022, according to the Centers for Disease Control and Prevention. Adverse reactions or quality problems associated with the use of this product may be reported to FDA's MedWatch Adverse Event Reporting program either by phone, on line, by regular mail or by fax. Most of the time, they shouldnt cause alarm. Over the course of the year, other states received multiple reports of drug-resistant Pseudomonas, including a report of a Washington man who died after suffering bloodstream infection linked to over-the-counter eye drops. The drops were manufactured in Arizona. As of March 14, 68 patients across 16 states were found to have contracted the bacteria, known as Pseudomonas aeruginosa. Pharmedica said that, as of March 3, it had not received any reports of illness or other adverse events from the use of the eye drops. The initial recall included Ezri Care Artificial Tears Lubricant Eye Drops and Desam Pharma Artificial Tears Lubricant Eye Drops. What to Know About the Recent Eye Drop Recalls - New York Times via F.D.A. The FDA has determined these issues indicate a lack of sterility assurance. Here's what you need to know about the flurry of eye drop recalls In addition to drops, the FDA has also recalled Global Pharma Healthcare Artificial Eye Ointment due to possible bacterial contamination. Eye drops recall at Walmart, CVS, Walgreens - All About Vision To date, Altaire has received no reports of adverse events, nor has Altaire obtained any out of specifications results including Sterility testing, for the products. Reboot. Sign up for our newsletter to get tips directly in your inbox. Product was distributed Worldwide by Purely Soothing LLC via online e-commerce and Trade shows (Ex. July 15, 2019 -- Altaire Pharmaceuticals, Inc., announces today that it is voluntarily recalling the over the counter (OTC) and prescription (Rx) drug products and lots, within expiry, it has manufactured and distributed under the Altaire label and trade dress during the time period as indicated below. Read on to learn more about a current list of recalled eye drops and symptoms of bacterial eye infections to consider. The Food and Drug Administration recently announced recalls of several eye drop brands linked to an outbreak of drug-resistant bacteria responsible for three deaths and multiple cases of people. If you have "artificial tears" eye drops in your home, check to make sure you don't have one of these recently recalled products. Refresh Plus Generic name: Carboxymethylcellulose [ kar-boks-ee-meth-il-SEL-yoo-lose ] Brand names: Artificial Tears, Biolle Gel Tears, Biolle Tears, GenTeal, Lubricating Plus Eye Drops, . Clear Eyes Redness Relief (Handy Pocket Pal), Product Size: 0.2 oz. About 117 million Americans used eye drops and eyewash in 2020, according to Statista, a market research firm. The product is labeled as follows (refer the Firm Press Release for a detailed product list containing affected lot numbers): RECOMMENDATION: Consumers who have the product with any of the lot numbers listed in the Firm Press Release should stop use of the product immediately and return it to the place of purchase. There have not been reports of illness or infection related to the product. The agency first warned of the outbreak in January, and it has now infected at least 68 people in 16 states. Try these 6 ways to slow memory decline and lower dementia risk. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product. Refresh Plus Preservative Free Lubricant Eye Drops - 70ct Sign up for our newsletter to get tips directly in your inbox. The product can be identified by the photos provided below. In 2017, the United States saw about 2,700 deaths related to Pseudomonas aeruginosa and 32,600 cases in hospitalized patients, according to CDC estimates. FDA encourages health care professionals and patients to report adverse events or quality problems with any medicine to FDAs MedWatch Adverse Event Reporting program: Consumers may also report adverse reactions by contacting FDAs Consumer Complaint Coordinators. Pharmedica USA in March recalled Purely Soothing, 15% MSM Drops out of concern that the product is not sterile. The UC Davis Eye Center has not seen any cases linked to the EzriCare drops, but infections have been reported in 12 states, including California. Pseudomonas aeruginosa is an aggressive bacterium that is found all over the environment, including in water, soil and human waste. New mortgage rules could lead to some homebuyers paying more, Dylan Mulvaney breaks silence on Bud Light backlash in new video, First Republic clients pulled $100 billion in deposits, Death toll climbs in outbreak linked to recalled eye drops as new treatment identified. People not experiencing symptoms do not need to test for possible infection, it says. While recalls are being implemented across the nation, cases thus far have been recorded in 16 states: California, Colorado, Connecticut, Florida, Illinois, Nevada, New Jersey, New Mexico, New York, North Carolina, Pennsylvania, South Dakota, Texas, Utah, Washington and Wisconsin. Signs of an allergic reaction, like rash; hives; itching; red, swollen, blistered, or peeling skin with or without fever; wheezing; tightness in the chest or throat; trouble breathing, swallowing, or talking; unusual hoarseness; or swelling of the mouth, face, lips, tongue, or throat. Bacteria in recalled eye drops linked to cases of vision loss - CNN Earlier in February, two distinct eye drop products were recalled and have been directly linked to a risk of bacterial infection Artificial Tears Lubricant Eye Drops branded by EzriCare and. Administration of a non-sterile product intended to be sterile may result in serious and potentially life threatening infections or death. Available for Android and iOS devices. March 7, 2023 -- Two manufacturers of eyedrops have recalled products over fears about contamination and sterility. With officials at the Centers for Disease Control and Prevention (CDC) issuing first warnings on the uptick in bacterial infections back in January 2023, CDC agents have now identified nearly 70 patients in 16 different states that have suffered drug-resistant infections and multiple symptoms.

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