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 ...
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 ...
This story was originally published on MedTech Dive. To receive daily news and insights, subscribe to our free daily MedTech Dive newsletter. Smiths Medical has recalled infusion pumps to update the ...
Development of an aid to decision-making form (ADF) integrated into a major institutional program in oncology: A tool to support care goal identification. Biomarker testing in non-small cell lung ...
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 ...
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 ...
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 ...
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