Infusion pumps have been plagued with multiple FDA recalls in recent years, and some of the pumps identified in the recalls are still in use, according to a report by DotMed. For example, 200,000 ...
The FDA has ordered a recall of Medtronic’s SynchroMed II implantable infusion pump, models 8637-20 and 8637-40, distributed between May 2004 and July 8, 2011, according to an FDA news release. The ...
Baxter Healthcare has issued a recall for some Spectrum infusion pumps due to a potential defect involving missing motor mounting screws, which could lead to interruptions, delays or incorrect dosing ...
Becton, Dickinson and Company’s BDX, or popularly known as BD, initiated the recall of its infusion pumps last month after customer reports indicated software issues, potentially leading to inaccurate ...
Hospira has issued a Class I recall on the Abbott Acclaim Infusion Pumps and Hospira Acclaim Encore Infusion Pumps, due to faulty door assemblies. Hospira has received customer reports of broke door ...
The U.S. Food and Drug Administration has classified a corrective action involving insulin pumps from Tandem Diabetes Care ...
US regulators have finalized a new set of recommendations intended to make infusion pumps safer and more reliable. In the US, medical devices can come to market in a variety of different ways. Some ...
Tandem Diabetes Care issued an urgent medical device correction to upgrade the software of its Tandem Mobi insulin pumps that ...
The U.S. Food and Drug Administration issued a Class I recall, the agency's most serious, for the Medfusion syringe pump, the third major FDA recall for the line of devices made in Oakdale. Smiths ...
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