FDA Recalls Welch Allyn AEDs
The FDA and Welch Allyn issued a Class I recall of 14,054 Automatic External Defibrillators (AED) and MRL JumpStart external defibrillators manufactured between October 2002 and January 2007.
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2009 Medical Equipment Standards
Starting January 1, 2009, The Joint Commission implemented the Standards Improvement Initiative (SII). This involved revisions to the format, structure, numbering, and wording of standards and EPs. Redundant or nonessential standards and elements of performance were deleted, and similar standards and EPs were consolidated. Some EPs were split into separate requirements, and scoring categories were […]
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Resources: Tracked
With the implementation of RTLS, the team at Southeastern has seen improved workflows and cost efficiencies
Read MoreCardinal 303 to Bring Infusion Pumps Up to Code
Cardinal Health 303 and the FDA have signed an amended consent decree to correct violations of current Good Manufacturing Practice (cGMP) requirements in the company’s infusion pumps.
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A Vision for Growth
Novant Health’s CEMP restructures, expands, and advances to manage triple growth
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