NELLCOR PURITAN BENNETT IRELAND UNLIMITED COMPANY
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Founded
1989-05-15
Website
Risk Signals
8567 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
2024-08-30 (frontiersin.org)
Predictors of cerebral blood flow during surgery in the Trendelenburg position, and their correlations to postoperative cognitive function
BackgroundIn robot-assisted laparoscopic prostatectomy surgery patients are tilted 30°–40° head-down. Knowledge of cerebral autoregulation and determinants o...
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2023-11-30 (massdevice.com)
Elon Musk denies Neuralink monkey death claims, U.S. lawmakers want SEC probe
Elon Musk has responded to claims of grisly deaths suffered by test monkeys as a result of his Neuralink venture's brain implant.
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2023-07-18 (propublica.org)
Steak Dinners, Sales Representatives, and Risky Procedures: Inside the Big Business of Clogged Arteries
The text messages, a whistleblower's lawsuit and an internal investigation reveal the extent to which Medtronic allegedly “groomed” physicians to abuse its vascular products on patients at a VA hospital.
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2023-07-05 (massdevice.com)
FTC critiques Medtronic's legal reasoning in antitrust case
The U.S. Federal Trade Commission wants to have a say in Applied Medical Resources' antitrust lawsuit against Medtronic.
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2023-07-04 (competitionpolicyinternational.com)
FTC Submits Amicus Brief On Antitrust Standards Regarding Bundling Arrangements
The Federal Trade Commission submitted a friend-of-the-court brief in the U.S. District Court for the Central District of California...
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2023-05-04 (massdevice.com)
Stryker faces another bribery investigation
Stryker says the U.S. Justice Dept. and Securities and Exchange Commission contacted the company over potential antibribery law violations.
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2023-02-15 (propublica.org)
Steak Dinners, Sales Reps and Risky Procedures: Inside the Big Business of Clogged Arteries
Text messages, a whistleblower lawsuit and an internal investigation reveal the lengths to which Medtronic, the world’s largest medical device company, allegedly “groomed” doctors to overuse its vascular products in patients at a veterans’ hospital.
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2022-07-07 (natlawreview.com)
GT Newsletter | Competition Currents | July 2022
The FTC issued two orders for public comment in June 2022 settling allegations that JAB Consumer Partners’$ 1.1 billion acquisition of SAGE Veterinary Partners and$ 1.65 billion acquisition of the parent of veterinary clinic owner Ethos violated
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2020-10-02 (fiercebiotech.com)
Medtronic caught up in DOJ ventilator antitrust probe dating back to Covidien deal: WSJ
The Department of Justice has begun investigating whether Medtronic’ s acquisitions curbed competition among manufacturers of ventilators—and potentially| The Department of Justice has begun investigating whether Medtronic’ s acquisitions curbed competition among manufacturers of ventilators
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2016-03-08 (massdevice.com)
Bill Hawkins on his time at Medtronic, Immucor and 25 years in the hot seat | DeviceTalks podcast
For nearly a quarter of a century, William “Bill” Hawkins sat in the corner office of medtech companies of all sizes, before stepping down from Immucor last year to become the Atlanta-based company’s lead director.
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2005-10-14 (informa.com)
Estech's AF (atrial fibrillation) ablation tools:
The US FDA has given Estech 510(k) clearance to sell its Cobra line of products for the surgical treatment of atrial fibrillation (AF). The tools, which were also recently cleared for sale in Europe, comprise the Cobra Adhere radiofrequency ablation system and the Cobra bipolar pacing probe. The
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(igj.nl)
FSN-FA1342, Medtronic Inc., Durepair Dura Regeneration Matrix
Medtronic was informed by the contract manufacturer (Integra LifeSciences Boston) that based on internal investigation they have identified issues with in-process and finished goods endotoxin testing. These issues may have resulted in the release of product with out-of-specification endotoxin levels
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