Baxter’s infusion pumps are in the crosshairs once again after cybersecurity software developer Rapid7 discovered multiple potential vulnerabilities in the devices. The Sigma Spectrum infusion pumps ...
Errors in the setup or management of some of Baxter International’s infusion pumps could result in overlooked blockages in the pumps, potentially leading to serious injury or even death, the ...
Baxter recalled over 277,000 infusion pumps due to the risk of the device failing to alarm users of repeated upstream occlusion events. The SIGMA Spectrum Infusion Pump with Master Drug Library ...
Infusion pumps are the most common connected medical devices in hospitals and "possess the lion's share" of cybersecurity risk, concluded Cynerio's January report. The Palo Alto Networks study, ...
The FDA labeled 22,769 Baxter drug infusion devices as a Class I recall after receiving reports of false upstream occlusion alarms, which can delay therapy. The two infusion pumps, SIGMA Spectrum ...
The pumps streamline the training clinicians need and help reduce the burden of properly operating multiple disparate pump platforms. Baxter's Novum IQ LVP supports high-volume infusions at faster ...
Infusion pumps have been plagued with multiple FDA recalls in recent years, and some of the pumps identified in the recalls are still in use, according to a report by DotMed. For example, 200,000 ...
CHICAGO, July 13 (Reuters) - The U.S. Food and Drug Administration ordered Baxter International Inc to recall all of its Colleague infusion pumps in use and provide a refund or no-cost replacement to ...
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