The FDA today declared that the recall of an emergency infusion device kit is the most serious type.
The recall covers three models of disposable sets made by Smisson-Cartledge Biomedical for its ThermaCor 1200 rapid infuser, which is used for fluid or bolus delivery. The system is made of a footswitch for hands-free fluid control, a fluid delivery device and a single-use disposable set with supply lines that can be used with intravenous (IV) bags or surgical equipment, according to the FDA.
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