ST. PAUL, Minn.--(BUSINESS WIRE)--Smiths Medical, a leading global medical device manufacturer, announced today it has received FDA 510(k) clearance to market its CADD ®-Solis pain management system ...
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 ...
MINNEAPOLIS, Dec. 12, 2022 /PRNewswire/ -- Smiths Medical issued an Urgent Medical Device Correction Letter to notify affected customers of two potential issues with CADD TM Infusion System Infusion ...
In its second safety alert this year, Smiths Medical has issued a letter to its customers detailing a pair of potential issues with the infusion sets used alongside its CADD line of infusion systems.
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