Search Results for: recall

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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