NELLCOR PURITAN BENNETT IRELAND UNLIMITED COMPANY
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Founded
1989-05-15
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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.
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Recent Articles about NELLCOR PURITAN BENNETT IRELAND UNLIMITED COMPANY
Live alerts from global media, monitored by Business Radar
2024-09-18 (medicaldevice-network.com)
FDA designates Class I recall of McGrath Mac laryngoscopes
Medtronic’s McGrath Mac laryngoscope has been recalled due to the risk of the device causing serious harm or death to a patient.
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2024-09-16 (statnews.com)
Most cardiovascular devices with serious safety recalls aren’t tested in patients
The new data comes as a government watchdog is looking into how the FDA authorizes medical devices and handles safety recalls.
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2024-09-13 (marketaccesstoday.com)
Medtronic Recalls McGrath MAC Laryngoscopes Due to Battery Overheating and Explosion Risk
Medtronic issued a recall for specific McGrath MAC Video Laryngoscopes, following reports that certain models pose a risk .
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2024-04-04 (sohuutritue.net.vn)
Not ensuring safety, a series of medical devices were recalled in Canada
The Canadian Health Directorate recently issued a decision to recall a series of medical devices due to concerns about the risks of seriously affecting patient health.
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2024-02-28 (medtechdive.com)
Medtronic's Covidien has another Class I recall for PB980 ventilators
The event adds to Medtronic’s ongoing product safety issues. In January, CEO Geoff Martha said addressing recalls and patient safety were a “top priority.”
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2023-12-20 (californiahealthline.org)
Deep Flaws in FDA Oversight of Medical Devices, and Patient Harm, Exposed in Lawsuits and Records - California Healthline
Thousands of medical devices are sold, and even implanted, with no safety tests.
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2023-11-16 (massdevice.com)
Baxter recalls some syringe pumps due to underdosing risk
The FDA determined that the recall of the Baxter (NYSE:BAX) Novum IQ syringe pump is Class 1, the most serious kind.
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2023-11-16 (drugdeliverybusiness.com)
Surmodics has positive data on multiple drug-coated balloons
Surmodics (Nasdaq:SRDX) today announced positive study results for two of its drug-coated balloon (DCB) technologies.
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2023-03-06 (massdevice.com)
Medtronic pulsed-field ablation system exceeds safety goal in study
Medtronic announced today that its PulseSelect pulsed-field ablation (PFA) system exceeded its safety performance goal.
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2022-12-17 (startribune.com)
Medtronic has seen 23 serious medical device recalls in two years
Company toughens up internal assessment of safety risks.
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2022-03-09 (fiercebiotech.com)
Medtronic, FDA expand HawkOne atherectomy recall to include TurboHawk Plus catheters
Medtronic and the FDA are expanding the reach of a Class I recall handed down in January for the medtech giant’s catheter designed to clear out clogged arteries. | The previous recall covered more than 95,000 devices for Medtronic’ s HawkOne system after it was discovered that the catheter’ s
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2022-02-07 (yahoo.com)
Medtronic Issues Voluntary Recall For TurboHawk Plus Directional Atherectomy System
Medtronic Plc (NYSE: MDT) has initiated a voluntary recall to customers related to the risk associated with tip damage caused by guidewire prolapse in its 6 French (6Fr) TurboHawk Plus Directional Atherectomy System. Recently, Medtronic issued a recall for the HawkOne Atherectomy system due to tip
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