Medtronic Heart Pump Recall Deemed LifeThreatening by FDA

Medtronic Heart Pump Recall Deemed Life-Threatening by FDA

The device that was recalled, called the HVAD System, takes over for a failing heart. One patient may have died because of a flaw where moisture can penetrate the mechanical pump through loose power or data connectors.  

Flaws with a heart device that Medtronic Plc bought last month as part of a $1 billion deal have been deemed potentially life-threatening by U.S. regulators.

The device, called the HVAD System, takes over for a failing heart. One patient may have died because of a flaw where moisture can penetrate the mechanical pump through loose power or data connectors, said Chris Garland, a spokesman for the company. Medtronic acquired the device with its purchase last month of HeartWare International.

Doctors and patients were first notified about the issue in May and June, with instructions to closely monitor the HVAD System for loose connections, the company said in a statement Friday. The U.S. Food and Drug Administration has since classified the issue a Class 1 recall, meaning the problem is potentially life-threatening. Recall designations are used to classify an issue’s severity, and doesn’t mean that the devices necessarily need to be removed from patients and replaced.

Almost all 8,799 patients who could be affected have been notified, and 308 controllers have been replaced, the company said.

Last month, the company recalled the pump kits that were in hospital inventories because they were vulnerable to electrical faults and connection failures from exposure to moisture. The company has recovered 323 of those 350 at-risk kits.

By Michelle Fay Cortez

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