FDA Hands Philips its 5th Class I Recall of the Year for Faulty Ventilators
Philips’ recent recall regarding certain BiPAP machines has been classified as a Class I recall, according to the U.S. FDA.
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Evaluating and Selecting Medical Equipment
Here, 24×7 Magazine Chief Editor Keri Stephens sits down with Scott Skinner, MBA, FACHE, director of capital equipment planning at Sodexo Healthcare and PhD candidate, who is conducting a survey about evaluating and selecting medical equipment.
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Medtronic Recalls Endotracheal Tubes for Risk of Airway Obstruction
Medtronic is recalling certain endotracheal tubes after receiving customer complaints about obstruction of the tubes while used on patients.
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Medtronic Insulin Pump System Has Cybersecurity Vulnerability, FDA Says
The U.S. FDA is alerting medical device users about a cybersecurity risk for the Medtronic MiniMed 600 Series Insulin Pump System.
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Stryker Receives FDA Clearance for Bone Tumor Ablation System
Stryker, a medical tech company, announced its OptaBlate bone tumor ablation system (OptaBlate) received 510(k) clearance from the U.S. FDA.
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