FDA Recalls Sigma Spectrum Infusion Pump Model 35700

FDA notified healthcare professionals of the class 1 recall of the SIGMA Spectrum Infusion Pump Model 35700, which is used to deliver fluids, solutions, drugs, agents, nutritionals, electrolytes, blood and blood products via parenteral, enteral, intravenous, intra-arterial, subcutaneous, epidural, or irrigation routes of administration. The units may fail suddenly, causing inaccurate flow conditions during use,… Learn More »