MEDTRONIC VASCULAR GALWAY UNLIMITED COMPANY
Location
Founded
1989-12-19
Website
Risk Signals
4873 news mentions monitored
Industry Context
This company is tracked across risk categories, including those related to its sector (e.g., Surgical and Medical Instruments and Apparatus, Drugs, Drug Proprietaries, and Druggists' Sundries), including supply chain integrity, ESG practices, labor disputes, and regulatory compliance.
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Recent Articles about MEDTRONIC VASCULAR GALWAY UNLIMITED COMPANY
Live alerts from global media, monitored by Business Radar
2025-04-23 (legalexaminer.com)
After Four Deaths, Medtronic Recalls Another Pipeline Embolization Device
The U.S. Food and Drug Administration (FDA) recently announced the Class 1 recall of Medtronic Pi
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2025-04-01 (medicaldevice-network.com)
Medtronic recalls flow-diverting stents
Medtronic's latest recall of the Pipeline Vantage 027 and 021 products is likely to result in revenue losses in the flow-diverting stents market.
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2025-03-31 (aha.org)
FDA recalls Medtronic Aortic Root Cannulas | News
The Food and Drug Administration has identified a Class I recall of Medtronic Aortic Root Cannulas due to a risk of unexpected loose material in the male luer used in the cannula.
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2025-03-31 (einnews.com)
Vascular Cannula Recall: Medtronic Removes Aortic Root Cannula Due to Unexpected Loose Material in the Male Luer - EIN Presswire
This recall involves removing certain devices from where they are used or sold. The FDA has identified this recall as the most serious type. This device may
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2025-03-21 (kienthuc.net.vn)
Recall of Medtronic neurological intervention
Medtronic's neurological intervention has been announced by the US Food and Drug Administration FDA for recovery due to 17 injuries and 4 deaths.
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2025-03-19 (medtechdive.com)
Medtronic recalls embolization devices tied to 17 injuries, 4 deaths |
Medtronic will remove one model of Pipeline Vantage devices from where they're used and sold and will update the instructions for another model.
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2025-03-18 (msn.com)
Medtronic slips after FDA notice on product recall
Shares of Medtronic (NYSE:MDT) reached a session low on Tuesday after the U.S. Food and Drug Administration (FDA) announced a product recall involving the...
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2025-03-18 (usnews.com)
FDA Classifies Recall of Medtronic Embolization Devices as 'Most Serious'
US News is a recognized leader in college, grad school, hospital, mutual fund, and car rankings. Track elected officials, research health conditions, and find news you can use in politics, business, health, and education.
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2025-03-17 (fda.gov)
Medtronic Removes Pipeline Vantage Embolization Devices, Updates IFU
The FDA has identified this recall as the most serious type. This recall involves: removing the Pipeline Vantage 027 device models from where they are used...
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