CME America Announces a Follow-Up on the Voluntary Recall of BodyGuard® Infusion System

Company Announcement Date: July 03, 2020

FDA Publish Date: July 08, 2020

Product Type: Medical Devices

Reason for Announcement: Use of the pump system potentially could cause over-infusion or under-infusion of therapy

Company Name: CME America

Brand Name: BodyGuard

Product Description: Infusion System Administration Set (infusion set)


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