The company will keep the systems on the market but is asking providers to check devices for visible cracks and return ...

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WASHINGTON, D.C. — The U.S. Food and Drug Administration has issued a Class I recall, the most serious type, on Medtronic’s ...

JIANGSU JUMAO X-CARE Medical Equipment Co. issued a recall for the JMC5A Ni/Tru-Aire-5 Oxygen Concentrator after incidents of spontaneous fires. These fires could cause burns or worse. Patients are ...

For instance, in addition to other Abbott devices, products made by Medtronic, Abiomed and Getinge have had recalls that left them in use. Recalls that leave what the FDA identifies as potentially ...

Medtronic thinks there’s no evidence that anyone using the pumps has been affected in this way, but says it has decided to recall the MiniMed 508 and MiniMed Paradigm series as a precaution and ...

A positive national coverage determination (NCD) would help Medtronic rewrite its story from one of abject failure to one that demonstrates the company’s grit. Recall that Medtronic acquired the ...

News, December 02, 2022 Alert Another Recall Related to Medtronic HVAD System The controller driveline boot cover of the HVAD system may harden over time, which could delay access to the driveline ...

The FDA’s recall notice describes the risk of cracks and leaks in the device stopcocks. Medtronic wrote to customers in November after receiving customer complaints about the stopcocks ...

Medtronic thinks there’s no evidence that anyone using the pumps has been affected in this way, but says it has decided to recall the MiniMed 508 and MiniMed Paradigm series as a precaution and ...