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Smiths Medical said it identified an issue where the CADD-Solis pump, under certain conditions, may trigger a false alarm. (Photo By Al Drago/CQ Roll Call) Smiths Medical has recalled ambulatory ...
In a letter to customers, Smiths Medical outlined two issues that have arisen with its CADD infusion sets, each of which could possibly lead to serious harm or death, since they can keep the infusion ...
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 ...
ROCHESTER HILLS, Mich.--(BUSINESS WIRE)--InfuSystem Holdings, Inc. (NYSE American: INFU) (“InfuSystem” or the “Company”), a leading national health care service provider, facilitating outpatient care ...
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 ...
Medical device maker ICU Medical changed the designs of infusion pumps made in Minnesota without properly clearing important regulatory checks after a recent recall, according to a Food and Drug ...
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