24x7 Magazine

For the past twenty years, 24x7 Magazine has been a trusted source for professionals in Healthcare Technology Management. It offers in-depth insights into technology, regulations, and industry developments, along with management tips and profiles of key figures in the field. Featuring carefully crafted articles from influential thought leaders, 24x7 dives deep into the most challenging topics facing the HTM sector.

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Olympus Launches New Endoscope Drying Cabinet

3 weeks ago | 24x7mag.com | Alyx Arnett

Olympus Corp has launched the ScopeLocker Air endoscope drying cabinet, offering a new drying option for healthcare facilities. Drying endoscope channels is a critical component of reprocessing. The ScopeLocker Air endoscope drying cabinet, manufactured by Capsa Healthcare and distributed by Olympus Corp, helps facilitate the drying process and is designed to meet society guidelines for endoscope drying and storage.
Cardinal Health Launches Single-Use Vital Signs Monitoring System

3 weeks ago | 24x7mag.com | Alyx Arnett

Cardinal Health has launched its multi-parameter, single-patient use vital signs monitoring cable and lead wire system, the Kendall DL Multi System, in the United States. The system enables continuous monitoring of cardiac activity, blood oxygen level, and temperature through one point of connection.
Contractor Arrested for Alleged Theft and Attempted Resale of Medical Equipment from Iowa Hospital

3 weeks ago | 24x7mag.com | Alyx Arnett

A contractor working at the construction site of a new University of Iowa hospital in North Liberty has been accused of stealing more than $60,000 worth of medical supplies and equipment, as well as construction equipment, and attempting to resell it online, according to WHO 13 Des Moines.
Medtronic Removes Tracheostomy Tube Over Risk of Flange Disconnection

3 weeks ago | 24x7mag.com | Alyx Arnett

Medtronic and its subsidiary, Covidien, are recalling the Shiley adult flexible tracheostomy tube with TaperGuard cuff reusable inner cannula as the tube may become dislodged or move out of place if the securement flange becomes disconnected, according to a medical device recall notification from the US Food and Drug Administration. This could prevent patient breathing and/or block the airway, which may lead to a serious or life-threatening emergency.
Baxter Issues Correction for Novum IQ Infusion Pump Over Underinfusion Risk

3 weeks ago | 24x7mag.com | Alyx Arnett

Baxter has issued a letter to affected customers recommending Novum IQ large volume pumps to be corrected prior to use due to a potential for underinfusion, according to a medical device recall notice from the US Food and Drug Administration (FDA). The correction is recommended if the device has been powered off with the administration set loaded, or after the “standby mode” feature has been activated.
Healthcare Leaders Embrace GenAI-But Most Aren’t Ready to Implement It, Survey Finds

3 weeks ago | 24x7mag.com | Alyx Arnett

A new 2025 Future Ready Healthcare Survey Report from Wolters Kluwer Health, conducted in partnership with the independent marketing research firm Ipsos, reveals that while healthcare professionals widely recognize the transformative potential of generative AI (GenAI), most organizations are not yet ready to harness its full value.
New Artificial Heart Technology Earns FDA Breakthrough Device Designation

3 weeks ago | 24x7mag.com | Alyx Arnett

BiVACOR, a clinical-stage medical device company developing a titanium Total Artificial Heart, announced that its device has received Breakthrough Device Designation from the US Food and Drug Administration (FDA). The designation supports the BiVACOR Total Artificial Heart as a bridge to transplant for adults with severe biventricular or univentricular heart failure where current treatments, including LVADs, are not viable.
FDA Flags Three Infusion Pump Corrections from Smiths Medical as Class I Recalls

3 weeks ago | 24x7mag.com | Alyx Arnett

The US Food and Drug Administration (FDA) has classified three recent safety notices from Smiths Medical regarding its CADD-Solis Ambulatory Infusion Pumps and CADD-Solis VIP pumps as Class I recalls—the agency’s most serious designation. The corrections involve updates to device instructions rather than product removals, but the FDA warns that failure to follow the new guidance could lead to serious injury or death depending on the clinical context and medication being infused.
First Patient Cases Performed with Remanufactured da Vinci Xi Instruments

3 weeks ago | 24x7mag.com | Alyx Arnett

Restore Robotics announced that Eugene Dickens, MD, FACS, at Hillcrest Medical Center in Tulsa, Okla, conducted the first-in-human use of a remanufactured da Vinci Xi robotic instrument on a patient using the newest model robotic surgical system, the da Vinci 5. In addition, Panama City Surgery Center performed the first-in-human use on a da Vinci Xi, which is the workhorse of the da Vinci robotics surgical systems.
Small Medical Practices Face Outsized Fallout from Health Data Breaches, Report Finds

3 weeks ago | 24x7mag.com | Alyx Arnett

In 2024, over 259 million Americans—roughly 81% of the population—had their protected health information (PHI) compromised from data breaches, and a new report from Patient Protect reveals that small, independent medical practices are bearing the brunt of the damage, often without recovery. The report, The Economics of ePHI Exposure: A Long-Term Impact Model of Healthcare Data Breaches, models breach-related losses over a 10-year horizon.