Consumer Lawyers

FDA recalls another CareFusion infusion pump

In Product Recalls on August 28, 2012 at 2:23 pm

U.S. health regulators announced a recall of CareFusion’s Alaris pump module Model 8100, saying a potential keypad malfunction in the infusion pump could cause serious injury or death.

The U.S. Food and Drug Administration said the affected pump modules, used for delivering a variety of fluids, drugs and blood products to patients, were manufactured between October 2011 and February 2012.

The FDA classified the action as a Class I recall on its website, meaning that the defective units could cause serious harm to a patient’s health.

Read more: http://www.foxnews.com/health/2012/08/23/fda-recalls-another-carefusion-infusion-pump/#ixzz24qoamjlh

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