The FDA in 2023 recommended against the use of some syringes originating from China as it investigated reports of leaks, ...
The U.S. Food and Drug Administration classified a recall of Teleflex's inflatable devices that increase blood supply to the heart muscle as "most serious". The devices are used in patients undergoing ...
The FDA has elevated a recall from Medline that has seen the device distributor pull tens of thousands of endotracheal tubes ...
The FDA recently labeled a recall of Abbott (NYSE: ABT) + Abbott Laboratories $105.79 1.58% Open 107.32 Day High 107.32 52 ...
Abbott is recalling a system monitor used with the Heartmate cardiac pump because screen display issues could pose a risk to patients. The Class 1 recall affects 4,842 ...
The Food and Drug Administration issued the alert Friday ... The same bacteria sparked recalls and shortages of infant formula in 2022 after it was detected at a major U.S. formula factory.
The Food and Drug Administration issued a voluntary recall earlier this week on Crecelac Infant Powdered Goat Milk Infant Formula after a sample collected from a Texas store tested positive for ...
Despite the recall, the FDA said the contamination “is not likely to cause adverse health consequences.” Fiji released a statement to USA Today, which read, “We conducted evaluations of the ...
Although the initial recall only affected around 70,000 cases, the FDA expanded that recall to encompass 1.9 million bottles of water. The Food and Drug Administration has announced an update to a ...
OptumHealth Care Solutions, a subsidiary of UnitedHealth Group, joined the manufacturer and the U.S. Food and Drug Administration ... recall. The Optum recall applies to 208 devices.
On February 20, 2024, Medline Industries, LP initiated a nationwide recall of 6 SubG Endotracheal Tubes with Subglottic Suction and 10 kits that contain these devices. The inflation tube and other ...