www.fdanews.com/articles/142493-mhra-issues-device-alert-for-respiration-monitor
MHRA Issues Device Alert for Respiration Monitor
December 14, 2011
The Medicines and Healthcare products Regulatory Agency issued a field safety notice for Hospira’s Plum A+ infusion pump due to a possible delay in therapy caused by continuous recycling and/or rebooting if the LED display settings are adjusted from the original default settings.