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B. Braun Medical, Inc. recalls Infusomat Space Volumetric Infusion Pump System
B. Braun Medical, Inc is recalling Infusomat Space Volumetric Infusion Pump System due to faulty occlusion alarms. On certain models, an occlusion alarm may sound when no occlusion exists, causing the pump to stop the delivery of medications, such as high-risk medications like vasopressors.
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.
Questions?
If you have questions about this recall, contact B. Braun Medical Inc. at 1-800-627-PUMP (1-800-627-7867).
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