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ST. PAUL, Minn.--(BUSINESS WIRE)--Smiths Medical, a leading global medical device manufacturer, announced today it received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to launch ...
FDA recently classified Smith Medicals recall of its CADD-Solis and CADD-Solis VIP Ambulatory Infusion Pumps as Class I after it was found that certain previous software versions may cause potential ...
MINNEAPOLIS--(BUSINESS WIRE)--Smiths Medical, a leading global medical device manufacturer, announced today it has received FDA 510(k) clearance on the CADD ®-Solis ambulatory infusion pump with ...
Smiths Medical has recalled ambulatory infusion pumps to provide updated use instructions to providers after identifying issues with potential false alarms as well as two other problems that could ...