MEDTRONIC VASCULAR GALWAY UNLIMITED COMPANY

Location

Founded

1989-12-19

Risk Signals

4962 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.

Recent Articles about MEDTRONIC VASCULAR GALWAY UNLIMITED COMPANY

Live alerts from global media, monitored by Business Radar

Medtronic Neurosurgery External Drainage and Monitoring Systems Recall Issued After Injury Reports -

2025-02-06 (aboutlawsuits.com)

Medtronic Neurosurgery External Drainage and Monitoring Systems Recall Issued After Injury Reports -

An urgent medical device notification has been issued for Medtronic Neurosurgery Becker and Exacta External Drainage and Monitoring Systems, following at least 15 reported injuries.

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Medtronic recalls 55K angiography guidewires that weren't sterilized before shipping

2021-07-06 (fiercebiotech.com)

Medtronic recalls 55K angiography guidewires that weren't sterilized before shipping

On the heels of a string of recalls that culminated in the total discontinuation of its HeartWare blood pump, Medtronic has issued yet another medical device recall. | So far, only two complaints pertaining to the guidewire have been filed with the agency, with no reports of related injuries or

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Hidden FDA reports detail harm caused by scores of medical devices

2019-03-07 (tampabay.com)

Hidden FDA reports detail harm caused by scores of medical devices

The Food and Drug Administration has let companies file reports of injuries and malfunctions outside a widely scrutinized public database

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FDA classifies Covidien field action for Trellis-6 and Trellis-8 systems as a Class 1 recall

2015-02-13 (vascularnews.com)

FDA classifies Covidien field action for Trellis-6 and Trellis-8 systems as a Class 1 recall

Medtronic announced today that a previously communicated global voluntary recall to address an issue with certain lots of its Trellis-6 and Trellis-8 peripheral infusion systems has now been classified as a Class 1 recall by the US Food and Drug Administration (FDA).

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FDA reports recall of Medtronic Hawk One atherectomy device

(bioworld.com)

FDA reports recall of Medtronic Hawk One atherectomy device

The FDA announced a class I recall of the Medtronic Hawk One directional atherectomy catheter system due to more than 160 reports of problems with the device’s guidewire. The catheter tip could break or separate when the guidewire prolapses, a problem that is associated with 55 injuries and no

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‘An incredible friend’: Medtronic employee donates kidney to co-worker

(medtronic.com)

‘An incredible friend’: Medtronic employee donates kidney to co-worker

When Mark Bubalo let his Facebook friends know he was looking for a kidney donor, he never thought a colleague would come forward

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