Medtronic has recalled certain Pipeline Vantage Embolization Devices with Shield Technology due to an increased risk of ...
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FDA tags Medtronic embolisation device recall as Class IThe US Food and Drug Administration (FDA) has tagged Medtronic’s recall of certain Pipeline Vantage embolisation devices as ...
Shares of Medtronic (NYSE:MDT) reached a session low on Tuesday after the U.S. Food and Drug Administration (FDA) announced a ...
Medtronic will remove one model of Pipeline Vantage devices from where they’re used and sold and will update the instructions ...
AdvaMed is urging Congress to address tariffs, streamline medtech coverage, update AI policies and improve FDA hiring.
In a notice posted to the agency’s website, the FDA noted that on January 30, 2025, Medtronic (MDT) Neurovascular sent all affected customers ...
Medical device recalls are essential to patient safety, addressing critical issues in devices that may pose health risks. Here are some of the latest recalls reported to the FDA: ...
BD, Medtronic and Abbott were among the top 10 medical device manufacturers with the highest number of late reports, the ...
As of late February, there were 147 medical device recall events and 20 of them, or 13.6%, were Class I, according to a Modern Healthcare report.
This recall involves removing devices from use and sale. According to the FDA notice, the device may cause serious injury of death if customers continue to use it. As a result of the recall, Philips ...
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Will ISRG Stock Drop Continue After da Vinci 5 Recall?Intuitive Surgical faces a Class 2 recall for its da Vinci 5 system due to a pedal issue. Will this affect its 2025 rollout?
Product recalls across key Australian industries increased by 14% in the second half of 2024 compared to the first half, ...
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