Recall of eye products
Webb23 feb. 2024 · The Food and Drug Administration recommended expanding a recall to include additional eye drop products due to possible contamination. The FDA now encourages the public to immediately stop using Delsam Pharma’s Artificial Eye … Webb3 apr. 2024 · 50,000 products were recalled of that ointment. It is unclear what bacteria the FDA turned up in its analysis and whether it matches the strain in the fatal outbreak.
Recall of eye products
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Webb17 mars 2024 · A rare strain of bacteria found in recalled eyedrops has been linked to dozens of infections, as well as cases of vision loss, surgical removal of eyeballs and one death. Global Pharma... Webb14 mars 2024 · The Food and Drug Administration (FDA) has recently recalled three brands of eye drops, including one that has been linked to serious infections, vision loss and a death. UC Davis Health experts share what you need to know. Consumers are …
Webb10 apr. 2024 · The company issued the recall “out of an abundance of caution.” “Consumers who might still have the recalled products in their refrigerators should discard and not consume them,” the FDA warned. Those who have questions or want to get a refund can contact the Fresh Express Consumer Response Center at (800) 242-5472. … Webb23 mars 2024 · Meanwhile, other recent eye drop recalls have not been linked to the outbreak. Select lots of Purely Soothing 15% MSM Drops and Brimonidine Tartrate Ophthalmic Solution did not list any illnesses or injuries from the products but "using …
Webb22 mars 2024 · More than 10 different brands of artificial tears have been recalled. Most cases have been linked to EzriCare and Delsam Pharma eye drops, made by India-based Global Pharma Healthcare. According to the CDC, the eye drops were contaminated with … WebbA drugmaker in India recalled another eye product amid a US outbreak of a drug-resistant bug. As of Tuesday, 58 people across 13 states had tested positive for the bug, and one person had died. The FDA said it has concerns about Global Pharma's manufacturing …
Webb13 apr. 2024 · This recall involves the Flo Smart Water Monitor Lithium-Ion Battery Back-Ups. The Flo Water Monitor Battery Backup device was an optional add-on accessory that could be purchased separately to extend certain features of Moen’s Flo Smart Water …
Webb8 mars 2024 · The drops from the Phoenix-based company are supposed to help with eye irritation and dry eyes. Nearly 2,900 bottles have been recalled. Per the Pharmedica recall notice, “Pharmedica USA LLC is advising customers to immediately stop using the product and return it to the place of purchase. infonetixWebb24 mars 2024 · Pharmaceutical firm Pharmedica USA on March recalled two lots of "Purely Soothing, 15% MSM Drops," also over sterility concerns. Pharmedica warned that patients who use the contaminated eye... infonet group slWebb24 feb. 2024 · Artificial Eye Ointment (mineral oil 15%, white petrolatum 83%, 3.5 grams / 1/8 oz.) is used as an eye lubricant and to relieve dryness of the eyes. The affected product is packaged in a white ... infonet healtheast employeeWebb13 apr. 2024 · Washington, D.C. --The U.S. Consumer Product Safety Commission (CPSC) and Luxor Workspaces LLC, of Waukegan, Illinois, are announcing the recall of about 84,700 plastic and metal audiovisual carts due to a serious tip-over hazard to children.In addition, approximately 1,650 audiovisual carts were sold in Canada. Three children have … infonet newWebb24 feb. 2024 · The eyedrops being recalled in 2024 have reportedly been imported from India and disturbed over the Internet. The FDA has warned Americans to avoid Delsam Pharma’s Artificial Eye Ointment, after issuing a warning about EzriCare Artificial Tears eyedrops earlier this month. Both over-the-counter products come from the … infonet healtheastWebb22 feb. 2024 · On Feb. 1, the CDC issued an alert about an outbreak of a drug-resistant strain of bacteria, Pseudomonas aeruginosa, linked to artificial tear products. To date, 58 patients across 13 states have... infonet health regionWebb8 apr. 2024 · 4.2M FreeStyle Libre glucose monitors recalled by FDA for risk of overheating, fire. The issue affects more than 4.2 million devices across the US, the FDA says. infonetiheart radio