BD's recall of Alaris infusion pumps following software issues has been classified as the most severe recall by the FDA. A suspension of sales may hurt the top line going forward.
Problematic software has been the cause of multiple infusion pump recalls in the medical device industry over the past few ...
The Food and Drug Administration has identified a Class I recall of Becton, Dickinson and Company BD Alaris Systems Manager and BD Care Coordination Engine Infusion Adapters due to reports that ...
Coca-Cola has issued a recall of over 10,000 cans of its Original Coca-Cola due to the possible presence of foreign material, ...
“When they came face-to-face, Biden did not immediately recognize his onetime rival for the party’s nomination,” write Allen ...
The US intelligence community’s annual threat assessment led with the threat from drug cartels for apparently the first time in the report’s nearly 20-year history, according to Senate ...
Q4 2024 Earnings Conference Call March 25, 2025 8:00 AM ETCompany ParticipantsRon Nixon - Executive Chairman and ...
The Food and Drug Administration (FDA) issued the Class II recall, which affects approximately 4,800 bags of the cheese. A customer walks out of an Aldi supermarket on August 17, 2023, in ...
The FDA has assigned the recall a Class II designation. The U.S. Food and Drug Administration has assigned its second-highest classification to an earlier recall involving some canned green beans ...
Most cases of TASS can be treated with steroids within a few days, although severe cases can lead to permanent damage to the ...
The move was initiated by the manufacturer, Great Lakes Cheese Co. Inc., on February 15, which prompted the FDA to issue a recall notice on March 19, per AllRecipes.com. The FDA alert was a ...