NELLCOR PURITAN BENNETT IRELAND UNLIMITED COMPANY
Location
Founded
1989-05-15
Website
Risk Signals
8570 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), including supply chain integrity, ESG practices, labor disputes, and regulatory compliance.
Filter risk signals by topic
Select a theme below to explore the company’s news mentions in specific risk areas.
Recent Articles about NELLCOR PURITAN BENNETT IRELAND UNLIMITED COMPANY
Live alerts from global media, monitored by Business Radar
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.
Read more
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
Read more
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
Read more
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).
Read more
(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
Read more