refresh plus eye drops recall

If you think you may have an eye infection, contact your eye care provider. A Retail Level recall is limited to product lots currently in inventory at the chain store. Shortly after the warning, EzriCare Artificial Tears, a preservative-free, over-the-counter product that many infected patients reported using, was recalled by its manufacturer. Product Description: Clear Eyes Redness Relief (Handy Pocket Pal)UPC#: 6-78112-15418-7 Product Size: 0.2 FL. The company also provided a phone number and website for people to request a recall/return packet.. Global Pharma Healthcare said in a a statementthat consumers who use the contaminated eye drops could go blind. The voluntary recall has since expanded to include over-the-counter and prescription eye care products sold under the Altaire brand name and products labeled exclusively for Accutome, Focus Laboratories, Grandall Distributing Co. Inc., Natural Ophthalmics, OCuSOFT, Prestige and TRP Co. Altair reports that to date it has not received any reports of adverse effects from the voluntarily recalled products, nor has Altaire found any out-of-specifications outcomes of sterility testing for the 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, . About 117 million Americans used eye drops and eyewash in 2020, according to Statista, a market research firm. / MoneyWatch. Shop Plus Lubricant Eye Drops - Value Size and read reviews at Walgreens. You should avoid kava and 9 other risky dietary supplements. A severe eye infection can feel similar to less threatening conditions such as dry eye disease and other autoimmune or inflammatory diseases of the eyes, experts caution. "Patients reported over 10 different brands of artificial tears and some patients used multiple brands," the CDC indicated. Altaire has notified Accutome, Focus Laboratories, Grandall Distributing Co. Inc. and Prestige by e-mail on July 16, 2019 announcing the recalls of the products/lots identified herein, with specific directions for return of all units of the impacted lots. There have been a total of three deaths linked back to exposure through eye drops specifically, with federal investigators indicating that they may soon learn of additional illnesses. The people who were sickened most commonly reported using EzriCare brand eye drops, while some patients used multiple brands. The company said that using the contaminated ointment could lead to infections that cause blindness, though it has not received any reports of injuries related to the product. Equate Restore Tears Lubricant Eye Drops Twin Pack, W-M item #: 552374320 NDC #: 49035-189-49 Package Size: 2 x 15 mL, W-M item #: 567371432 NDC #: 49035-887-13 Package Size: 15 mL, W-M item #: 563031651 NDC #: 49035-875-50 Package Size: 3.5 gram, Equate Comfort Gel Lubricant Eye Gel Twin Pack, W-M item #: 552374319 NDC #: 49035-197-49 Package Size: 2 x 15 mL, Equate Restore PM Nighttime Lubricant Eye Ointment, W-M item #: 551282425 NDC #: 49035-191-50 Package Size: 3.5 gram, Equate Night & Day Restore Tears Lubricant Eye Pack, W-M item #: 567368000 NDC #: 49035-883-59 Package Size: 3.5g and 15mL, W-M item #: 567371433 NDC #: 49035-885-49 Package Size: 2 x 15 mL, Equate Support Advanced Lubricating Eye Drops Dose Preservative Free. More eye drops are being recalled. Allergan recalls Refresh, FML, Blephamide eye drops CDC issued an alert recommending consumers stop using EzriCare Artificial Tears pending additional guidance from CDC and FDA. How to Safely Use Eye Drops After the EzriCare Recall - Verywell Health But when medical products such as eye drops become contaminated, the concentration of bacteria or viruses, or fungi in the product can be extremely high and overwhelm local immune responses, even when people are not overtly immune compromised, he said. Weeks later, two other types of eye drops were recalled because they posed a different kind of contamination risk. Bacteria in recalled eye drops linked to cases of vision loss - CNN Teva Pharmaceuticals have set up a recall hotline at 888-838-2872 for shoppers who have additional questions. Patients who suffered infections of Pseudomonas aeruginosa reported using more than 10 brands of artificial tears, but none as often as EzriCare, according to the CDC. The company said it initiated the recall "out of an abundance of caution" over concerns that cracks in some of the units' caps could compromise the drops' sterility and lead to infection. Why Trust Us? As a precautionary measure, Altaire is initiating the recall due to management concerns regarding the sufficiency of Quality Assurance controls over critical systems in the manufacturing facility. Purely Soothing, 15% MSM Drops were recalled due to non-sterility. He has written about food and dining for Time, among other publications. 2023 CBS Interactive Inc. All Rights Reserved. The eye drops could be contaminated, according to the recall, and may be associated with the CDC's ongoing investigation into "extensively drug-resistant" infections that weren't responsive. Altaire ships the products labeled for Accutome, Focus Laboratories, Grandall Distributing Co. Inc. and Prestige only to Accutome, Focus Laboratories, Grandall Distributing Co. Inc. and Prestige, respectively. If a patient experiences eye pain, swelling, ocular discomfort or irritation after using any of the recalled products, Allergan says the patient should contact a healthcare provider. Angelika Warmuth/Picture-Alliance-DPA, via Associated Press, The manufacturer of EzriCare Artificial Tears said it was recalling the product out of an abundance of caution.. Other steps to prevent eye infections include making sure to wash your hands before touching your eyes or eye drops. But the flurry of recalls is leaving some regular users of the products wondering, are they safe? Eye drops recall at Walmart, CVS, Walgreens - All About Vision These are over-the-counter products, manufactured by Global Pharma Healthcare Private Limited, intended to be sterile. Look down and gently . UC Davis Health experts share what you need to know. Apotex recalled six lots of Brimonidine Tartrate Ophthalmic Solution 0.15 percent prescription eye drops. This recall is being conducted with the knowledge of the U.S. Food and Drug Administration. The Phoenix-based company said consumers should immediately stop using the drops and return them to the place they were purchased. 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. This recall is being carried out to the retail level and is only for the specific lots listed above. The products are distributed at the retail level by Walgreens. Pharmedica is recalling its Purely Soothing 15% MSM Drops meant to treat eye irritation. What Happened To Refresh Repair Eye Drops? - On Secret Hunt Oz. The companies involved in the recalls are Phoenix-based Pharmedica and Florida-based Apotex. Oz. The hospital that reported the first infection determined it was caused by the Pseudomonas aeruginosa bacteria, which can cause infections in the blood, lungs or other parts of the body. Refresh Plus Lubricant Eye drops instantly moisturizes and relieves dry, irritated eyes with a fast-acting, long-lasting formula for sensitive eyes that has many of the same healthy qualities as your own natural tears. Customers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product. Two More Brands of Eyedrops Recalled Over Infection Risks - US News Global Pharma Healthcare is voluntarily recalling all lots within expiry of their Artificial Tears Lubricant Eye Drops, distributed by /EzriCare, LLC- and Delsam Pharma, to the consumer level,. Pseudomonas aeruginosa, which occurs naturally in the environment, can spread to humans who are exposed to contaminated water or soil. Additional eye drop recalls are making headlines this month, but it's important to note that they are not expressly related to bacterial infections being linked to Pseudomonas aeruginosa. Pharmaceutical firmPharmedica USA on Marchrecalled two lots of "Purely Soothing, 15% MSM Drops," also over sterility concerns. Here's what you need to know about the flurry of eye drop recalls Earlier this year, there were at least two distinct recalls that were linked to potential bacterial contamination, with CDC agents indicating that EzriCare Artificial Tears were most commonly cited in the bulk of reported infections thus far. Apotex is recalling six lots of Brimonidine Tartrate Ophthalmic Solution 0.15% - prescription eye drops used to treat open-angle glaucoma or ocular hypertension. In addition to the three deaths that are being traced back to tainted eye drops, CNN reports that federal officials have indicated that eight patients have developed blindness due to the outbreak. TO DATE, ALTAIRE HAS NOT OBTAINED ANY OUT OF SPECIFICATION RESULTS, INCLUDING IN-HOUSE AND THIRD-PARTY STERILITY TESTING, FOR THESE PRODUCTS. Symptoms associated with bacterial eye infections can include a wide array of eye-related discomfort and pain, including yellow, green or clear discharge; redness of the eye or eyelid; increased light sensitivity; consistent blurry vision; as well as an unshakable inner-eye irritation that feels like an itch, according to CDC officials. How older drivers can improve their driving at night, Accutome, Focus Laboratories, Grandall Distributing, How to find the best eye drops for your symptoms. Read on to learn which eye drops are being recalled and why. Dry eye disease is one of the most common eye diseases and can cause irritation, grittiness, redness, burning, tearing and blurred vision. 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. "If we don't really need something, then we probably shouldn't be using it. Best preservative-free eye drops: Refresh Optive Mega-3. 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. The foregoing products are manufactured and labeled by Altaire Pharmaceuticals, Inc. Altaire has notified all distributors by e-mail on July 15, 2019 announcing the recalls of the products/lots identified herein, with specific directions for return of all units of the impacted lots. The drops were manufactured in Arizona. ICE Limitations. Apotex recalled six lots of Brimonidine Tartrate Ophthalmic Solution 0.15 percent prescription eye drops. Oz. CDC Posts Update to Investigation Into Infections Linked to Eye Drops It was later expanded to include Delsam Pharma Artificial. It has . Pharmedica "Purely Soothing, 15% MSM Drops." Well+Being shares news and advice for living well every day. 2 Manufacturers Recall Eyedrops Over Safety Concerns - WebMD Administration of a non-sterile product intended to be sterile may result in serious and potentially life threatening infections or death. Consumers with questions regarding this recall can contact the distributor Delsam Pharma, LLC by phone at 1-866-826-1306 or by e-mail at delsampharma@yahoo.com from Monday to Friday from 11am to 4pm EST. Apotex "Brimonidine Tartrate Ophthalmic Solution, 0.15%." We're recapping that information below. REFRESH PLUS Lubricant Eye Drops instantly moisturizes and relieves mild symptoms of eye dryness, including burning, irritation, and discomfort. Here's what you need to know about the flurry of eye drop recalls OZ. Patients who have signs or symptoms of an eye infection should talk to their health care provider or seek medical care immediately. Its also important to check the expiration date. Most of the time, they shouldnt cause alarm. July 5, 2019 -- Altaire Pharmaceuticals, Inc., announces today that it is voluntarily recalling the Over-the-Counter (OTC) drug products and lots, within expiry, sold at Wal-Mart during the time period as indicated in the tables below. Change in eyesight, eye pain, or very bad eye irritation. First published on March 8, 2023 / 5:32 PM. Wholesalers and retailers should stop distributing/return to Pharmedica USA LLC immediately or confirm that the product has been disposed of with proper verification. The symptoms can include yellow, green or clear discharge from the eye, redness of the eye or eyelid, increased sensitivity to light and eye pain or discomfort. has also warned people to stop using an eye ointment manufactured by Global Pharma because of possible contamination. NDC#: 59390-175-35 Product Size: 4 Fl. The outbreak has also been connected to eight recent reports of vision loss and four reports of enucleation, or surgical removal of an eyeball. Teva Pharmaceuticals have set up a recall hotline at 888-838-2872 for shoppers who have additional questions. As of January 31, 2023, CDC identified 55 patients in 12 states with infections that have been linked by epidemiologic and laboratory evidence to use of EzriCare Artificial Tears. No other lots are being recalled. Common side effects of Refresh may include: mild eye burning or irritation; itching or redness of your eyes; watery eyes; blurred vision; or sensitivity to light. The recall came after the Centers for Disease Control and Prevention (CDC) began an investigation of a cluster of multistate bacterial infections it believed were associated with the tear drops. In January, testing confirmed the Florida cases were caused by the same bacteria strain as cases in California, Connecticut and Utah. If it's not a real problem maybe we have a tiny bit of dryness we probably shouldn't be putting something into our eye," he said. 0.15% and were sold between last April through February. TO DATE ALTAIRE HAS NOT RECEIVED ANY REPORTS OF ADVERSE EVENTS FOR THE PRODUCTS.TO DATE ALTAIRE HAS NOT OBTAINED ANY OUT OF SPECIFICATIONS RESULTS, INCLUDING IN-HOUSE AND THIRD PARTY STERILITY TESTING, FOR THE PRODUCTS. Available for Android and iOS devices. To safely apply eye drops, she said, people should use their nondominant hand to gently tug on the lower eyelid, look up slightly, and then, with the dominant hand, put that little drop in that lower cul-de-sac in the eyelid area.. If you have "artificial tears" eye drops in your home, check to make sure you don't have one of these recently recalled products. Updated on: March 24, 2023 / 10:49 AM In January, the Centers for Disease Control and Prevention and the Food and Drug Administration warned people to stop using EzriCare Artificial Tears and Delsam Pharmas Artificial Tears after the eye drops were linked to a drug-resistant strain of the bacteria Pseudomonas aeruginosa. To date, Global Pharma Healthcare has not received any reports of adverse events related to this product.

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refresh plus eye drops recall