Smiths Medical, a Minneapolis-based medical device-maker, is recalling its Medfusion syringe pumps after discovering a software issue that could cause the pumps’ low battery alarms to stop working.
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KORU Medical secures certification under EU MDR for infusion pump
The certification expands access to Freedom60 and FreedomEDGE infusion pumps for growing SCIg prefilled syringe use.
Drug pumps used widely in the US contain severe security vulnerabilities which could allow hackers to administer fatal doses, a researcher claims. Billy Rios, a security expert who has been testing ...
A syringe pump made by a Minneapolis-based company is being recalled for risks that could cause life-threatening injuries or death. The Food and Drug Administration (FDA) issued a Class I correction ...
The U.S. government is taking a closer look at how to stop hackers from taking control of medical devices like pacemakers. An inspector general's report last month found the Food and Drug ...
Please provide your email address to receive an email when new articles are posted on . Zyno Medical is recalling select infusion pumps due to a software defect that may cause air bubbles to be passed ...
Medical device company Medtronic is recalling a number of insulin pumps after discovering they are vulnerable to hacks — and there’s no way to patch the security holes. The FDA announced the ...
Smiths Medical has issued a Class I recall for certain CADD-Solis and CADD-Solis VIP ambulatory infusion pumps due to multiple issues that could interrupt or delay medication delivery. The FDA ...
- Will introduce first level of its gamified training application developed by Level Ex, developers of the Level One diabetes-management game SAN DIEGO, CA / ACCESS Newswire / August 8, 2025 / Modular ...
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KORU Medical secures EU MDR certification for Freedom60 infusion pump
KORU Medical Systems, Inc. KRMD recently announced that its Freedom60 Infusion Pump — along with an adapter designed for 50 ...
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