1. Impact of Vapotherm Recall On Patient Care in the NICU Introduction: The Vapotherm 2000i device was recalled due to a possible association with Ralstonia bacteria colonization. Approximately 5000 devices used on approximately 120,000 patients per year where removed from over 800 US medical centers.... www.rcjournal.com
2. Vapotherm 2000i (Respiratory Gas Humidifier System) [Posted 02/01/2007] FDA notified healthcare professionals of the reintroduction of the 2000i Respiratory Gas Humidifier System. This system was recalled in 2005 due to possible contamination with Ralstonia spp. cultures. FDA noted that premature n... www.fda.gov
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