Nearly 43,000 Defibrillators Recalled Over Power Problem

Physio-Control Inc. is recalling some models of external defibrillators because of a possible failure of battery power, the Food and Drug Administration said. The battery problem in the device may have led to the death of one person.

Defibrillators are used to shock the heart of a patient in cardiac arrest.

The recall includes approximately 42,943 Physio-Control LIFEPAK 20 and LIFEPAK 20e external defibrillators that were manufactured from July 31, 2002 to September 19, 2007.

Instead of removing the devices from the market, the company is trying to fix the defibrillators in the field, and is urging frequent testing until corrections can be made.

According to the company, battery failure is unlikely and hospital employees generally usually plug the device into the wall, The Wall Street Journal reports.

“While there have been reports of failures during patient use, over the eight-year product life, there has been one unconfirmed adverse patient event,” the company said in a press release.

Physio-Control is notifying its customers by mail, and will update the power system free of charge.

In April, the company took action to fix a different defibrillator model. Brian Webster, Physio-Control’s president, told The Journal that the recalls are “signs of a healthy quality system.”

Customers can call the company at 1-800-442-1142.

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