Colombian Navy workers are accused of helping drug traffickers place tracking devices aboard Colombian Navy vessels.
The FDA recall affects more than 25,000 of the Fridley-run company’s devices and follows reports of 17 injuries.
The state is using roadside tests to check whether drivers have used drugs, similar to tests for alcohol. A pilot program found that 87 percent of tested drivers had used cannabis or illegal drugs.
The Food and Drug Administration has identified a Class I recall of Medtronic Neurovascular 027 Compatible Pipeline Vantage ...
Minnesota law enforcement officers tried out two devices that can detect six classes of drugs and chemicals that can impair ...
The recall, which affects two models of Pipeline Vantage embolization devices, is linked to 17 injuries and four deaths.
Medical Device Network on MSN3d
FDA tags Medtronic embolisation device recall as Class IMedtronic initiated the recall of certain Pipeline Vantage embolisation devices in January 2025 following reports of four ...
The FDA deemed a recall of some Medtronic Pipeline Vantage embolization devices serious after multiple deaths related to the ...
The U.S. Food and Drug Administration on Tuesday classified the recall of Medtronic's embolization device as "most serious", ...
The FDA announced that Medtronic initiated a device recall and correction for embolization devices. The FDA has identified ...
BD, Medtronic and Abbott were among the top 10 device companies with the highest number of late reports to the FDA, the study ...
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