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All product recalls associated with Datex-Ohmeda Inc One Ohmeda.
Total Recalls
4
Past Year
0
Class I (Serious)
0
Most Recent
Apr 2004
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Increased circuit pressure as a result of a misassembled Aestiva/5 Active Gas Scavenging System.
Anesthetic agents could be delivered at concentrations above the concentration set on the S/5 and AS/3 Anesthesia Delivery Units (ADU) having serial numbers within a specified range.
Datex-Ohmeda Cardiocap/5 Patient Monitors have bracket pins which do not adequately secure them to their optional mounting stand so the monitors may fall.