WebFeb 27, 2024 · The U.S. Food and Drug Administration (FDA) has expanded its eye drops and ointment recall and told consumers to stop using Delsam Pharma’s Artificial Eye Ointment due to a possible contamination with bacteria that has been linked to cases of blinding. India-based Global Pharma Healthcare Private Limited, the manufacturer for … WebAffected customers are being instructed to verify products implicated in these recalls by checking UPC codes on the eye drop's exterior packaging, which has been detailed in FDA recall announcements.
2 More Eye Drop Brands Recalled Due to Safety Risks
WebApr 8, 2024 · At least 7 fires and one injury that were related to some FreeStyle Libre glucose monitor products have led the FDA to issue a Class I recall The issue affects … WebMar 1, 2024 · On Wednesday, the U.S. Food and Drug Administration ( FDA ) said that Global Pharma adhered to the agency’s request to recall Delsam Pharma’s Artificial Eye Ointment, an over-the-counter product. “FDA recommended that Global Pharma recall Delsam Pharma’s Artificial Eye Ointment, and the firm agreed to initiate a recall,” … relation ftp pma
FreeStyle Libre recall: FDA warns of risk of lithium-ion batteries ...
WebApr 12, 2024 · The biggest themes lately have been Philips ventilator recalls, contaminated eye drops, and prohibiting Juul from selling e-cigs. Beyond that, it’s been a “slow news cycle” for FDA lately. WebFeb 22, 2024 · The over-the-counter product is made by the same company that makes eye drops that were recalled earlier this year amid an outbreak of a highly drug-resistant bacteria that has hospitalized and ... WebApr 8, 2024 · Some FreeStyle Libre glucose monitors recalled for risk of fire: FDA Sterilization issue found at recalled eye drop manufacturer's facility Popular hoverboards recalled due to fire risk, 2 deaths relation force poids