CME America Announces a Follow-Up on the Voluntary Recall of BodyGuard® Infusion System Administration Sets
Date of publication: 03-07-2020
As part of CME America's commitment to quality, following the previously announced recall (April 27, 2020) of the BodyGuard® Infusion Pump Systems, the company conducted additional flow-rate accuracy testing. This testing revealed that some infusion sets do not meet the ±5% delivery accuracy for the Źródło: http://www.fda.gov
