ResMed Begins Worldwide Recall of CPAP Devices
ResMed has initiated a voluntary worldwide recall of approximately 300,000 S8 flow generators used for treating obstructive sleep apnea.
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The EC.9.10 Standard
The January and March 2007 “CCE Prep” articles in 24×7 reviewed the requirements of the two main Joint Commission medical equipment standards, EC.6.10 and EC.6.20. This article will review the EC.9.10 Joint Commission standard that links with the medical equipment management program. Managing a comprehensive medical equipment program requires knowing more than the two main […]
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The Joint Commission Medical Equipment Standards
In January 2007, the Joint Commission on Accreditation of Healthcare Organizations, or JCAHO, officially shortened its name to “The Joint Commission.” The CCE Prep article in the January 2007 issue of 24×7 reviewed the requirements of The Joint Commission standard EC.6.10. This article will review the requirements of standard EC.6.20. Each Joint Commission standard is […]
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An Active Role
With a commitment to training, innovation, and collaboration, the clinical engineering department at SLU has increased its visibility
Read MoreFDA Warns for Proper Use of Reintroduced Vapotherm Devices
The FDA has issued a Public Health Notification urging users to exercise caution when using the reintroduced Vapotherm 2000i respiratory Gas Humidifier System.
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