Baxter Removes Sigma Spectrum Infusion System Platforms
The removal is tied to incorrect software installations that could result in inaccurate flow rates and user confusion during clinical use.
The removal is tied to incorrect software installations that could result in inaccurate flow rates and user confusion during clinical use.
The FDA issued an early alert under its recall communications pilot citing 79 injuries and two deaths linked to Baxter’s Novum IQ infusion pump.
Issues may cause therapy delays, false alarms, or thermal damage, though no injuries reported to date.
The removal is tied to incorrect software installations that could result in inaccurate flow rates and user confusion during clinical use.
With the clearances, ICU Medical introduces its new category of infusion devices, designed to address infusion delivery variability.
Read MoreBD is correcting software for its Alaris Systems Manager and CCE Infusion Adapter after identifying a risk that outdated infusion parameters could be uploaded, potentially leading to incorrect dosing.
Read MoreThe FDA has issued an early alert regarding Baxter’s recall of certain Spectrum infusion pumps due to missing motor mounting screws, which may have occurred during servicing.
Read MoreAccurate Biomed will support CAIRE customers with in-warranty repairs, including the FreeStyle Comfort portable oxygen concentrator and the company’s line of stationary oxygen concentrator products.
Read MoreBaxter is recalling certain Solution Sets with Duo-Vent Spikes due to an assembly issue that led to inverted slide clamps.
Read MoreFresenius Kabi recalled a specific lot of Ivenix LVP Primary Administration Sets due to a defect that could cause uncontrolled flow.
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Inspira Technologies introduced the INSPIRA Cardi-ART, a portable modular device that provides oxygen to the brain during cardiac arrest.