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 ...

MINNEAPOLIS--(BUSINESS WIRE)--Smiths Medical, a leading global medical device manufacturer of specialty infusion devices, announced today that its CADD-Solis v3.0 PIB Ambulatory Infusion Pump has ...

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 ...

A medical device correction has been issued by Smiths Medical for its CADD-Solis and CADD-Solis VIP infusion pumps due to software issues. The recall, which involves correcting devices and not ...

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 ...

Today, Smiths Medical’s correction of the CADD-Solis Li-ion rechargeable battery packs was deemed FDA Class I. The CADD-Solis Li-ion rechargeable battery packs are lithium-ion battery packs used as an ...