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 ...

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 ...

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 ...

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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 ...

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 ...

FDA Clears Smiths Medical to Market Patient-Controlled Pain Pump The U.S. Food and Drug Administration has given St. Paul, Minn.-based Smiths Medical 510 (k) clearance to market its CADD-Solis Pain ...

A newly launched pain management system aims to maintain effective epidural analgesia in post-operative pain management patients through programmed intermittent bolus medication delivery. Smiths ...