The Food and Drug Administration has categorized Smiths Medical’s correction of more than 50,000 syringe pumps in the U.S. as a Class I recall. Smiths Medical, which became part of ICU Medical in a $2 ...

Smiths Medical, a Minneapolis-based medical device-maker, is recalling its Medfusion syringe pumps after discovering a software issue that could cause the pumps’ low battery alarms to stop working.

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urging healthcare providers to update tens of thousands of its hospital syringe pumps after identifying issues with outdated software, and now the FDA is helping to get the ...

A syringe pump made by a Minneapolis-based company is being recalled for risks that could cause life-threatening injuries or death. The Food and Drug Administration (FDA) issued a Class I correction ...

New York, Aug. 09, 2021 (GLOBE NEWSWIRE) -- Reportlinker.com announces the release of the report "Infusion Pumps - Medical Devices Pipeline Product Landscape, 2021 ...

Smiths Medical has warned customers of more than 135,000 Medfusion syringe pumps about problems associated with earlier software versions. On March 5, the FDA posted an alert for 85,961 Medfusion ...

This tutorial discusses critical considerations requiring attention when designing an infusion pump, including FDA regulation, self-test circuitry, and meeting the IEC 60601-1 standard for electrical ...

Download the full report: https://www.reportbuyer.com/product/3878535/?utm_source=PRN GlobalData's Medical Devices sector report, "Implantable Infusion Pumps ...

Smiths Medical Inc., of Minneapolis, has undertaken a recall of its Medfusion 3500 and 4000 series of syringe infusion pumps because of software issues that could lead to over- or under-infusion of ...