The U.S. FDA has categorized a recall of Abbot pacemakers caused by a manufacturing process that allowed moisture into the devices as a Class I event; some devices containing the fault could still be in use, reports MedTech Dive.
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Pacific Medical Group is recalling the Alaris Infusion Pump Module Model 8100 because the front bezel components may crack or separate.
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The alert provides recommended safety actions healthcare organizations can take to reduce the risks of errors caused by the misuse of smart infusion pumps.
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Medtronic has recalled the Valiant Navion thoracic stent graft system due to stent fractures and endoleak concerns. But the FDA has categorized the recall as Class 1, the most critical kind.
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Executives from Siemens Healthineers, Health-ISAC, and Irdeto recently hosted a virtual panel discussion regarding ways medical device manufacturers can build cybersecurity into their processes. Here are a few takeaways from the roundtable discussion.
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