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 ...

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, announced today it has received FDA 510(k) clearance on the CADD ®-Solis ambulatory infusion pump with ...

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 ...

The FDA gave 510(k) clearance to Smiths Medical's "smart" infusion pump, which includes error-prevention software for a number of therapies. The company says its CADD-Solis VIP pump improves on the ...

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 ...

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 ...

Minneapolis-based Smiths Medical Inc., recalled two entries in the company’s CADD-Solis line of ambulatory infusion pumps due to problems with the preloaded software.

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.

Smiths Medical, a leading global medical device manufacturer, announced an agreement today with Epic to develop connectivity between the company’s infusion systems and Epic’s Electronic Medical ...

Smiths Medical has been urging healthcare providers to update tens of thousands of its hospital syringe pumps after identifying issues with outdated software, and now the FDA is helping to get the ...